ENST00000291281.9:c.512G>T
MANE Select
|
ENSP00000291281.3:p.Gly171Val
|
|
ENST00000291281.8:c.512G>T
|
ENSP00000291281.3:p.Gly171Val
|
|
ENST00000433867.5:c.512G>T
|
ENSP00000393978.1:p.Gly171Val
|
|
ENST00000595132.5:c.41G>T
|
ENSP00000470363.1:p.Gly14Val
|
|
ENST00000595515.5:c.512G>T
|
ENSP00000470804.1:p.Gly171Val
|
|
ENST00000597641.1:c.247G>T
|
ENSP00000469064.1:n.247G>T
|
|
ENST00000598633.1:c.41G>T
|
ENSP00000470919.1:p.Gly14Val
|
|
ENST00000600194.5:c.41G>T
|
ENSP00000472744.1:p.Gly14Val
|
|
ENST00000601605.5:c.41-3537G>T
|
ENSP00000470442.1:n.41-3537G>T
|
|
ENST00000601806.5:c.41G>T
|
ENSP00000469106.1:p.Gly14Val
|
|
NM_001079880.1:c.512G>T
|
NP_001073349.1:p.Gly171Val
|
|
NM_001079881.1:c.512G>T
|
NP_001073350.1:p.Gly171Val
|
|
NM_001079882.1:c.41G>T
|
NP_001073351.1:p.Gly14Val
|
|
NM_016457.4:c.512G>T
|
NP_057541.2:p.Gly171Val
|
|
XM_005258716.2:c.41G>T
|
XP_005258773.2:p.Gly14Val
|
|
NM_001079880.2:c.512G>T
|
NP_001073349.1:p.Gly171Val
|
|
NM_001079881.2:c.512G>T
|
NP_001073350.1:p.Gly171Val
|
|
NM_001079882.2:c.41G>T
|
NP_001073351.1:p.Gly14Val
|
|
NM_016457.5:c.512G>T
MANE Select
|
NP_057541.2:p.Gly171Val
|
|