ENST00000461574.2:c.5424T>A
|
ENSP00000417241.2:p.Val1808=
|
|
ENST00000470026.6:c.5427T>A
|
ENSP00000419274.2:p.Val1809=
|
|
ENST00000473961.6:c.5301T>A
|
ENSP00000420201.2:p.Val1767=
|
|
ENST00000476777.6:c.5421T>A
|
ENSP00000417554.2:p.Val1807=
|
|
ENST00000477152.6:c.5349T>A
|
ENSP00000419988.2:p.Val1783=
|
|
ENST00000478531.6:c.2115T>A
|
ENSP00000420412.2:p.Val705=
|
|
ENST00000489037.2:c.5349T>A
|
ENSP00000420781.2:p.Val1783=
|
|
ENST00000493919.6:c.1977T>A
|
ENSP00000418819.2:p.Val659=
|
|
ENST00000494123.6:c.5427T>A
|
ENSP00000419103.2:p.Val1809=
|
|
ENST00000497488.2:c.4539T>A
|
ENSP00000418986.2:p.Val1513=
|
|
ENST00000618469.2:c.5427T>A
|
ENSP00000478114.2:p.Val1809=
|
|
ENST00000634433.2:c.5304T>A
|
ENSP00000489431.2:p.Val1768=
|
|
ENST00000644379.2:c.5493T>A
|
ENSP00000496570.2:p.Val1831=
|
|
ENST00000644555.2:c.1977T>A
|
ENSP00000494614.2:p.Val659=
|
|
ENST00000652672.2:c.5286T>A
|
ENSP00000498906.2:p.Val1762=
|
|
ENST00000484087.6:c.1989T>A
|
ENSP00000419481.2:p.Val663=
|
|
ENST00000700081.1:n.1310T>A
|
|
|
ENST00000700082.1:n.791T>A
|
|
|
ENST00000357654.9:c.5427T>A
MANE Select
|
ENSP00000350283.3:p.Val1809=
|
|
ENST00000471181.7:c.5490T>A
|
ENSP00000418960.2:p.Val1830=
|
|
ENST00000644379.1:c.1814T>A
|
|
|
ENST00000352993.7:c.2001T>A
|
ENSP00000312236.5:p.Val667=
|
|
ENST00000357654.7:c.5427T>A
|
ENSP00000350283.3:p.Val1809=
|
|
ENST00000461221.5:c.*5210T>A
|
ENSP00000418548.1:n.*5210T>A
|
|
ENST00000468300.5:c.2041T>A
|
ENSP00000417148.1:p.Cys681Ser
|
|
ENST00000471181.6:c.5490T>A
|
ENSP00000418960.2:p.Val1830=
|
|
ENST00000491747.6:c.2115T>A
|
ENSP00000420705.2:p.Val705=
|
|
ENST00000493795.5:c.5286T>A
|
ENSP00000418775.1:p.Val1762=
|
|
ENST00000586385.5:c.357T>A
|
ENSP00000465818.1:p.Val119=
|
|
ENST00000591534.5:c.900T>A
|
ENSP00000467329.1:p.Val300=
|
|
ENST00000591849.5:c.126T>A
|
ENSP00000465347.1:p.Val42=
|
|
NM_007294.3:c.5427T>A , LRG_292t1:c.5427T>A
|
NP_009225.1:p.Val1809=
|
|
NM_007297.3:c.5286T>A
|
NP_009228.2:p.Val1762=
|
|
NM_007298.3:c.2115T>A
|
NP_009229.2:p.Val705=
|
|
NM_007299.3:c.2041T>A
|
NP_009230.2:p.Cys681Ser
|
|
NM_007300.3:c.5490T>A
|
NP_009231.2:p.Val1830=
|
|
NR_027676.1:n.5563T>A
|
|
|
NM_007294.4:c.5427T>A
MANE Select
|
NP_009225.1:p.Val1809=
|
|
NM_007297.4:c.5286T>A
|
NP_009228.2:p.Val1762=
|
|
NM_007299.4:c.2041T>A
|
NP_009230.2:p.Cys681Ser
|
|
NM_007300.4:c.5490T>A
|
NP_009231.2:p.Val1830=
|
|
NR_027676.2:n.5604T>A
|
|
|