ENST00000263038.9:c.760G=
MANE Select
|
ENSP00000263038.4:p.Asp254=
|
|
ENST00000263038.8:c.760G=
|
ENSP00000263038.4:p.Asp254=
|
|
ENST00000396913.6:c.460G=
|
ENSP00000380121.2:p.Asp154=
|
|
ENST00000396920.7:c.709G=
|
ENSP00000380126.3:p.Asp237=
|
|
ENST00000453759.6:c.460G=
|
ENSP00000412525.2:p.Asp154=
|
|
NM_001037537.1:c.460G=
|
NP_001032626.1:p.Asp154=
|
|
NM_006214.3:c.760G=
|
NP_006205.1:p.Asp254=
|
|
XM_005252469.2:c.541G=
|
XP_005252526.1:p.Asp181=
|
|
NM_001323080.1:c.460G=
|
NP_001310009.1:p.Asp154=
|
|
NM_001323082.1:c.766G=
|
NP_001310011.1:p.Asp256=
|
|
NM_001323083.1:c.496G=
|
NP_001310012.1:p.Asp166=
|
|
NM_001323084.1:c.466G=
|
NP_001310013.1:p.Asp156=
|
|
NM_006214.4:c.760G=
MANE Select
|
NP_006205.1:p.Asp254=
|
|
NM_001037537.2:c.460G=
|
NP_001032626.1:p.Asp154=
|
|
NM_001323080.2:c.460G=
|
NP_001310009.1:p.Asp154=
|
|
NM_001323082.2:c.766G=
|
NP_001310011.1:p.Asp256=
|
|
NM_001323083.2:c.496G=
|
NP_001310012.1:p.Asp166=
|
|
NM_001323084.2:c.466G=
|
NP_001310013.1:p.Asp156=
|
|