ENST00000263038.9:c.760G>C
MANE Select
|
ENSP00000263038.4:p.Asp254His
|
|
ENST00000263038.8:c.760G>C
|
ENSP00000263038.4:p.Asp254His
|
|
ENST00000396913.6:c.460G>C
|
ENSP00000380121.2:p.Asp154His
|
|
ENST00000396920.7:c.709G>C
|
ENSP00000380126.3:p.Asp237His
|
|
ENST00000453759.6:c.460G>C
|
ENSP00000412525.2:p.Asp154His
|
|
NM_001037537.1:c.460G>C
|
NP_001032626.1:p.Asp154His
|
|
NM_006214.3:c.760G>C
|
NP_006205.1:p.Asp254His
|
|
XM_005252469.2:c.541G>C
|
XP_005252526.1:p.Asp181His
|
|
NM_001323080.1:c.460G>C
|
NP_001310009.1:p.Asp154His
|
|
NM_001323082.1:c.766G>C
|
NP_001310011.1:p.Asp256His
|
|
NM_001323083.1:c.496G>C
|
NP_001310012.1:p.Asp166His
|
|
NM_001323084.1:c.466G>C
|
NP_001310013.1:p.Asp156His
|
|
NM_006214.4:c.760G>C
MANE Select
|
NP_006205.1:p.Asp254His
|
|
NM_001037537.2:c.460G>C
|
NP_001032626.1:p.Asp154His
|
|
NM_001323080.2:c.460G>C
|
NP_001310009.1:p.Asp154His
|
|
NM_001323082.2:c.766G>C
|
NP_001310011.1:p.Asp256His
|
|
NM_001323083.2:c.496G>C
|
NP_001310012.1:p.Asp166His
|
|
NM_001323084.2:c.466G>C
|
NP_001310013.1:p.Asp156His
|
|