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. 2018 May 8;8:7255. doi: 10.1038/s41598-018-25491-9

Figure 1.

Figure 1

The diagram shows the amino acid (top) and codon (bottom) identities for the Wild Type and R1 mutant alleles of SfABCC2. The R1 mutant has a 2 bp GC insertion (highlighted in red) in the 740th codon, which causes a premature stop codon to arise at codon 747.