ENST00000461574.2:c.5459T=
|
ENSP00000417241.2:p.Phe1820=
|
|
ENST00000470026.6:c.5462T=
|
ENSP00000419274.2:p.Phe1821=
|
|
ENST00000473961.6:c.5336T=
|
ENSP00000420201.2:p.Phe1779=
|
|
ENST00000476777.6:c.5456T=
|
ENSP00000417554.2:p.Phe1819=
|
|
ENST00000477152.6:c.5384T=
|
ENSP00000419988.2:p.Phe1795=
|
|
ENST00000478531.6:c.2150T=
|
ENSP00000420412.2:p.Phe717=
|
|
ENST00000489037.2:c.5384T=
|
ENSP00000420781.2:p.Phe1795=
|
|
ENST00000493919.6:c.2012T=
|
ENSP00000418819.2:p.Phe671=
|
|
ENST00000494123.6:c.5462T=
|
ENSP00000419103.2:p.Phe1821=
|
|
ENST00000497488.2:c.4574T=
|
ENSP00000418986.2:p.Phe1525=
|
|
ENST00000618469.2:c.5462T=
|
ENSP00000478114.2:p.Phe1821=
|
|
ENST00000634433.2:c.5339T=
|
ENSP00000489431.2:p.Phe1780=
|
|
ENST00000644379.2:c.5528T=
|
ENSP00000496570.2:p.Phe1843=
|
|
ENST00000644555.2:c.2012T=
|
ENSP00000494614.2:p.Phe671=
|
|
ENST00000652672.2:c.5321T=
|
ENSP00000498906.2:p.Phe1774=
|
|
ENST00000484087.6:c.2024T=
|
ENSP00000419481.2:p.Phe675=
|
|
ENST00000700081.1:n.1345T=
|
|
|
ENST00000700082.1:n.826T=
|
|
|
ENST00000357654.9:c.5462T=
MANE Select
|
ENSP00000350283.3:p.Phe1821=
|
|
ENST00000471181.7:c.5525T=
|
ENSP00000418960.2:p.Phe1842=
|
|
ENST00000644379.1:c.1849T=
|
|
|
ENST00000352993.7:c.2036T=
|
ENSP00000312236.5:p.Phe679=
|
|
ENST00000357654.7:c.5462T=
|
ENSP00000350283.3:p.Phe1821=
|
|
ENST00000461221.5:c.*5245T=
|
ENSP00000418548.1:n.*5245T=
|
|
ENST00000468300.5:c.2076T=
|
ENSP00000417148.1:p.Leu692=
|
|
ENST00000471181.6:c.5525T=
|
ENSP00000418960.2:p.Phe1842=
|
|
ENST00000491747.6:c.2150T=
|
ENSP00000420705.2:p.Phe717=
|
|
ENST00000493795.5:c.5321T=
|
ENSP00000418775.1:p.Phe1774=
|
|
ENST00000586385.5:c.392T=
|
ENSP00000465818.1:p.Phe131=
|
|
ENST00000591534.5:c.935T=
|
ENSP00000467329.1:p.Phe312=
|
|
ENST00000591849.5:c.161T=
|
ENSP00000465347.1:p.Phe54=
|
|
NM_007294.3:c.5462T= , LRG_292t1:c.5462T=
|
NP_009225.1:p.Phe1821=
|
|
NM_007297.3:c.5321T=
|
NP_009228.2:p.Phe1774=
|
|
NM_007298.3:c.2150T=
|
NP_009229.2:p.Phe717=
|
|
NM_007299.3:c.2076T=
|
NP_009230.2:p.Leu692=
|
|
NM_007300.3:c.5525T=
|
NP_009231.2:p.Phe1842=
|
|
NR_027676.1:n.5598T=
|
|
|
NM_007294.4:c.5462T=
MANE Select
|
NP_009225.1:p.Phe1821=
|
|
NM_007297.4:c.5321T=
|
NP_009228.2:p.Phe1774=
|
|
NM_007299.4:c.2076T=
|
NP_009230.2:p.Leu692=
|
|
NM_007300.4:c.5525T=
|
NP_009231.2:p.Phe1842=
|
|
NR_027676.2:n.5639T=
|
|
|