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. 2020 Aug 26;21:591. doi: 10.1186/s12864-020-07004-z

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© The Author(s) 2020

Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

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Fig. 5 — Cell-based functional testing of DGAT1 K232A influence on splicing efficiency at the DGAT1 intron 7 junction. a represents the splicing ratio (spliced transcripts:unspliced transcripts) measured by qPCR in each of the individual replicates for the intron 7 junction. b represents the average splicing ratio for the intron 7 junction for the two DGAT1 K232A alleles. The error bars represent the standard deviation across all samples. c and d represent the mean spliced and unspliced transcripts for the intron 7 junction, respectively. The error bars represent the standard error of the difference between means