ENST00000461574.2:c.5390T>A
|
ENSP00000417241.2:p.Phe1797Tyr
|
|
ENST00000470026.6:c.5393T>A
|
ENSP00000419274.2:p.Phe1798Tyr
|
|
ENST00000473961.6:c.5267T>A
|
ENSP00000420201.2:p.Phe1756Tyr
|
|
ENST00000476777.6:c.5387T>A
|
ENSP00000417554.2:p.Phe1796Tyr
|
|
ENST00000477152.6:c.5315T>A
|
ENSP00000419988.2:p.Phe1772Tyr
|
|
ENST00000478531.6:c.2081T>A
|
ENSP00000420412.2:p.Phe694Tyr
|
|
ENST00000489037.2:c.5315T>A
|
ENSP00000420781.2:p.Phe1772Tyr
|
|
ENST00000493919.6:c.1943T>A
|
ENSP00000418819.2:p.Phe648Tyr
|
|
ENST00000494123.6:c.5393T>A
|
ENSP00000419103.2:p.Phe1798Tyr
|
|
ENST00000497488.2:c.4505T>A
|
ENSP00000418986.2:p.Phe1502Tyr
|
|
ENST00000618469.2:c.5393T>A
|
ENSP00000478114.2:p.Phe1798Tyr
|
|
ENST00000634433.2:c.5270T>A
|
ENSP00000489431.2:p.Phe1757Tyr
|
|
ENST00000644379.2:c.5459T>A
|
ENSP00000496570.2:p.Phe1820Tyr
|
|
ENST00000644555.2:c.1943T>A
|
ENSP00000494614.2:p.Phe648Tyr
|
|
ENST00000652672.2:c.5252T>A
|
ENSP00000498906.2:p.Phe1751Tyr
|
|
ENST00000484087.6:c.1955T>A
|
ENSP00000419481.2:p.Phe652Tyr
|
|
ENST00000700081.1:n.1276T>A
|
|
|
ENST00000357654.9:c.5393T>A
MANE Select
|
ENSP00000350283.3:p.Phe1798Tyr
|
|
ENST00000471181.7:c.5456T>A
|
ENSP00000418960.2:p.Phe1819Tyr
|
|
ENST00000644379.1:c.1780T>A
|
|
|
ENST00000352993.7:c.1967T>A
|
ENSP00000312236.5:p.Phe656Tyr
|
|
ENST00000357654.7:c.5393T>A
|
ENSP00000350283.3:p.Phe1798Tyr
|
|
ENST00000461221.5:c.*5176T>A
|
ENSP00000418548.1:n.*5176T>A
|
|
ENST00000468300.5:c.2021-1431T>A
|
ENSP00000417148.1:n.2021-1431T>A
|
|
ENST00000471181.6:c.5456T>A
|
ENSP00000418960.2:p.Phe1819Tyr
|
|
ENST00000491747.6:c.2081T>A
|
ENSP00000420705.2:p.Phe694Tyr
|
|
ENST00000493795.5:c.5252T>A
|
ENSP00000418775.1:p.Phe1751Tyr
|
|
ENST00000586385.5:c.323T>A
|
ENSP00000465818.1:p.Phe108Tyr
|
|
ENST00000591534.5:c.866T>A
|
ENSP00000467329.1:p.Phe289Tyr
|
|
ENST00000591849.5:c.92T>A
|
ENSP00000465347.1:p.Phe31Tyr
|
|
NM_007294.3:c.5393T>A , LRG_292t1:c.5393T>A
|
NP_009225.1:p.Phe1798Tyr
|
|
NM_007297.3:c.5252T>A
|
NP_009228.2:p.Phe1751Tyr
|
|
NM_007298.3:c.2081T>A
|
NP_009229.2:p.Phe694Tyr
|
|
NM_007299.3:c.2021-1431T>A
|
NP_009230.2:n.2021-1431T>A
|
|
NM_007300.3:c.5456T>A
|
NP_009231.2:p.Phe1819Tyr
|
|
NR_027676.1:n.5529T>A
|
|
|
NM_007294.4:c.5393T>A
MANE Select
|
NP_009225.1:p.Phe1798Tyr
|
|
NM_007297.4:c.5252T>A
|
NP_009228.2:p.Phe1751Tyr
|
|
NM_007299.4:c.2021-1431T>A
|
NP_009230.2:n.2021-1431T>A
|
|
NM_007300.4:c.5456T>A
|
NP_009231.2:p.Phe1819Tyr
|
|
NR_027676.2:n.5570T>A
|
|
|