ENST00000461574.2:c.5560A=
|
ENSP00000417241.2:p.Ile1854=
|
|
ENST00000470026.6:c.5563A=
|
ENSP00000419274.2:p.Ile1855=
|
|
ENST00000473961.6:c.5437A=
|
ENSP00000420201.2:p.Ile1813=
|
|
ENST00000476777.6:c.5557A=
|
ENSP00000417554.2:p.Ile1853=
|
|
ENST00000477152.6:c.5485A=
|
ENSP00000419988.2:p.Ile1829=
|
|
ENST00000478531.6:c.2251A=
|
ENSP00000420412.2:p.Ile751=
|
|
ENST00000489037.2:c.5485A=
|
ENSP00000420781.2:p.Ile1829=
|
|
ENST00000493919.6:c.2113A=
|
ENSP00000418819.2:p.Ile705=
|
|
ENST00000494123.6:c.5563A=
|
ENSP00000419103.2:p.Ile1855=
|
|
ENST00000497488.2:c.4675A=
|
ENSP00000418986.2:p.Ile1559=
|
|
ENST00000618469.2:c.5563A=
|
ENSP00000478114.2:p.Ile1855=
|
|
ENST00000634433.2:c.5440A=
|
ENSP00000489431.2:p.Ile1814=
|
|
ENST00000644379.2:c.5629A=
|
ENSP00000496570.2:p.Ile1877=
|
|
ENST00000644555.2:c.2113A=
|
ENSP00000494614.2:p.Ile705=
|
|
ENST00000652672.2:c.5422A=
|
ENSP00000498906.2:p.Ile1808=
|
|
ENST00000484087.6:c.2125A=
|
ENSP00000419481.2:p.Ile709=
|
|
ENST00000700081.1:n.1446A=
|
|
|
ENST00000700082.1:n.927A=
|
|
|
ENST00000357654.9:c.5563A=
MANE Select
|
ENSP00000350283.3:p.Ile1855=
|
|
ENST00000471181.7:c.5626A=
|
ENSP00000418960.2:p.Ile1876=
|
|
ENST00000644379.1:c.1950A=
|
|
|
ENST00000352993.7:c.2137A=
|
ENSP00000312236.5:p.Ile713=
|
|
ENST00000357654.7:c.5563A=
|
ENSP00000350283.3:p.Ile1855=
|
|
ENST00000461221.5:c.*5346A=
|
ENSP00000418548.1:n.*5346A=
|
|
ENST00000468300.5:c.*77A=
|
ENSP00000417148.1:n.*77A=
|
|
ENST00000471181.6:c.5626A=
|
ENSP00000418960.2:p.Ile1876=
|
|
ENST00000491747.6:c.2251A=
|
ENSP00000420705.2:p.Ile751=
|
|
ENST00000493795.5:c.5422A=
|
ENSP00000418775.1:p.Ile1808=
|
|
ENST00000586385.5:c.493A=
|
ENSP00000465818.1:p.Ile165=
|
|
ENST00000591534.5:c.1036A=
|
ENSP00000467329.1:p.Ile346=
|
|
ENST00000591849.5:c.262A=
|
ENSP00000465347.1:p.Ile88=
|
|
NM_007294.3:c.5563A= , LRG_292t1:c.5563A=
|
NP_009225.1:p.Ile1855=
|
|
NM_007297.3:c.5422A=
|
NP_009228.2:p.Ile1808=
|
|
NM_007298.3:c.2251A=
|
NP_009229.2:p.Ile751=
|
|
NM_007299.3:c.*77A=
|
NP_009230.2:n.*77A=
|
|
NM_007300.3:c.5626A=
|
NP_009231.2:p.Ile1876=
|
|
NR_027676.1:n.5699A=
|
|
|
NM_007294.4:c.5563A=
MANE Select
|
NP_009225.1:p.Ile1855=
|
|
NM_007297.4:c.5422A=
|
NP_009228.2:p.Ile1808=
|
|
NM_007299.4:c.*77A=
|
NP_009230.2:n.*77A=
|
|
NM_007300.4:c.5626A=
|
NP_009231.2:p.Ile1876=
|
|
NR_027676.2:n.5740A=
|
|
|