ENST00000461574.2:c.4633G>T
|
ENSP00000417241.2:p.Asp1545Tyr
|
|
ENST00000470026.6:c.4636G>T
|
ENSP00000419274.2:p.Asp1546Tyr
|
|
ENST00000473961.6:c.4510G>T
|
ENSP00000420201.2:p.Asp1504Tyr
|
|
ENST00000476777.6:c.4630G>T
|
ENSP00000417554.2:p.Asp1544Tyr
|
|
ENST00000477152.6:c.4558G>T
|
ENSP00000419988.2:p.Asp1520Tyr
|
|
ENST00000478531.6:c.1324G>T
|
ENSP00000420412.2:p.Asp442Tyr
|
|
ENST00000489037.2:c.4558G>T
|
ENSP00000420781.2:p.Asp1520Tyr
|
|
ENST00000493919.6:c.1186G>T
|
ENSP00000418819.2:p.Asp396Tyr
|
|
ENST00000494123.6:c.4636G>T
|
ENSP00000419103.2:p.Asp1546Tyr
|
|
ENST00000497488.2:c.3748G>T
|
ENSP00000418986.2:p.Asp1250Tyr
|
|
ENST00000618469.2:c.4636G>T
|
ENSP00000478114.2:p.Asp1546Tyr
|
|
ENST00000634433.2:c.4513G>T
|
ENSP00000489431.2:p.Asp1505Tyr
|
|
ENST00000644379.2:c.4702G>T
|
ENSP00000496570.2:p.Asp1568Tyr
|
|
ENST00000644555.2:c.1186G>T
|
ENSP00000494614.2:p.Asp396Tyr
|
|
ENST00000652672.2:c.4495G>T
|
ENSP00000498906.2:p.Asp1499Tyr
|
|
ENST00000484087.6:c.1198G>T
|
ENSP00000419481.2:p.Asp400Tyr
|
|
ENST00000700182.1:c.1243G>T
|
ENSP00000514849.1:p.Asp415Tyr
|
|
ENST00000357654.9:c.4636G>T
MANE Select
|
ENSP00000350283.3:p.Asp1546Tyr
|
|
ENST00000471181.7:c.4699G>T
|
ENSP00000418960.2:p.Asp1567Tyr
|
|
ENST00000644379.1:c.1023G>T
|
|
|
ENST00000352993.7:c.1210G>T
|
ENSP00000312236.5:p.Asp404Tyr
|
|
ENST00000357654.7:c.4636G>T
|
ENSP00000350283.3:p.Asp1546Tyr
|
|
ENST00000461221.5:c.*4419G>T
|
ENSP00000418548.1:n.*4419G>T
|
|
ENST00000468300.5:c.1324G>T
|
ENSP00000417148.1:p.Asp442Tyr
|
|
ENST00000471181.6:c.4699G>T
|
ENSP00000418960.2:p.Asp1567Tyr
|
|
ENST00000478531.5:c.1324G>T
|
ENSP00000420412.1:p.Asp442Tyr
|
|
ENST00000484087.5:c.949G>T
|
ENSP00000419481.1:p.Asp317Tyr
|
|
ENST00000491747.6:c.1324G>T
|
ENSP00000420705.2:p.Asp442Tyr
|
|
ENST00000493795.5:c.4495G>T
|
ENSP00000418775.1:p.Asp1499Tyr
|
|
ENST00000493919.5:c.1186G>T
|
ENSP00000418819.1:p.Asp396Tyr
|
|
ENST00000586385.5:c.5-10419G>T
|
ENSP00000465818.1:n.5-10419G>T
|
|
ENST00000591534.5:c.109G>T
|
ENSP00000467329.1:p.Asp37Tyr
|
|
ENST00000591849.5:c.-98-24180G>T
|
ENSP00000465347.1:n.-98-24180G>T
|
|
NM_007294.3:c.4636G>T , LRG_292t1:c.4636G>T
|
NP_009225.1:p.Asp1546Tyr
|
|
NM_007297.3:c.4495G>T
|
NP_009228.2:p.Asp1499Tyr
|
|
NM_007298.3:c.1324G>T
|
NP_009229.2:p.Asp442Tyr
|
|
NM_007299.3:c.1324G>T
|
NP_009230.2:p.Asp442Tyr
|
|
NM_007300.3:c.4699G>T
|
NP_009231.2:p.Asp1567Tyr
|
|
NR_027676.1:n.4772G>T
|
|
|
NM_007294.4:c.4636G>T
MANE Select
|
NP_009225.1:p.Asp1546Tyr
|
|
NM_007297.4:c.4495G>T
|
NP_009228.2:p.Asp1499Tyr
|
|
NM_007299.4:c.1324G>T
|
NP_009230.2:p.Asp442Tyr
|
|
NM_007300.4:c.4699G>T
|
NP_009231.2:p.Asp1567Tyr
|
|
NR_027676.2:n.4813G>T
|
|
|