Table 7. Splicing events correlated to change in transcripts known splice isoforms.

Genes	P-value	Gene description	Log Fold change	Gene description	Log fold change
NF2	0.0129	NF2, transcript variant 5	3.87	NF2, transcript variant 8	−0.71
PCNX	0.0099	PCNX, transcript variant X10	3.59	PCNX, transcript variant X2	−1.67
SRPK2	0.043	SRPK2, transcript variant 2	3.32	SRPK2, transcript variant X3	−2.68
FAM73A	0.0139	FAM73A, transcript variant 1	3.09	FAM73A, transcript variant X3	−2.86
MTHFD2L	0.0179	MTHFD2L, transcript variant X2	2.73	MTHFD2L, transcript variant X1	−0.38
ABHD2	0.0242	ABHD2, transcript variant X1	2.51	ABHD2, transcript variant X2	−1.34
C1orf27	0.0196	C1orf27, transcript variant 3	2.17	C1orf27, transcript variant X4	−1.29
NAE1	0.0055	NAE1, transcript variant X2	1.93	NAE1, transcript variant 2	−0.99
SMEK2	0.0288	SMEK2, transcript variant X6	1.80	SMEK2, transcript variant X7	−0.09
FBXO38	0.0356	FBXO38, transcript variant 3	1.75	FBXO38, transcript variant X3	−1.17
FKBP14	0.0362	FKBP14, transcript variant 2, non-coding RNA	1.74	FKBP14, RefSeqGene (LRG_454) on chromosome 7	−0.02
GTF2H1	0.0475	GTF2H1, transcript variant 2	1.64	GTF2H1, transcript variant X1	−0.50
HUWE1	0.0004	HUWE1, transcript variant X5	1.59	HUWE1, transcript variant X2	−0.28
SLC38A9	0.0457	SLC38A9, transcript variant X2	1.59	SLC38A9, transcript variant X8, misc_RNA	−0.62
SLC7A11	0.0174	SLC7A11	1.57	SLC7A11 transcript variant X1	−0.04
SRGAP2	0.0091	SRGAP2, transcript variant X7	1.47	SRGAP2, RefSeqGene on chromosome 1	−0.22
ADAM19	0.0346	ADAM19	1.47	ADAM19, transcript variant X1	−0.23
FANCL	0.0354	FANCL, transcript variant X5, misc_RNA	1.42	LRG_501 on chromosome 2	−0.35
FOSL1	0.0433	FOSL1, transcript variant 1	1.40	FOSL1, transcript variant 5	−1.39