ENST00000585465.3:c.*2894G=
|
ENSP00000490268.2:n.*2894G=
|
|
ENST00000585748.3:c.921G=
|
ENSP00000477641.2:p.Lys307=
|
|
ENST00000585851.2:c.1119G=
|
ENSP00000467912.2:p.Lys373=
|
|
ENST00000326873.12:c.1293G=
MANE Select
|
ENSP00000324856.6:p.Lys431=
|
|
ENST00000326873.11:c.1293G=
|
ENSP00000324856.6:p.Lys431=
|
|
ENST00000585465.2:n.3026G=
|
|
|
ENST00000586243.5:c.1290G=
|
ENSP00000467240.2:p.Lys430=
|
|
ENST00000589152.5:n.1991G=
|
|
|
NM_000455.4:c.1293G= , LRG_319t1:c.1293G=
|
NP_000446.1:p.Lys431=
|
|
XM_005259617.1:c.1288G=
|
XP_005259674.1:p.Ala430=
|
|
XM_011528209.1:c.1066G=
|
XP_011526511.1:p.Ala356=
|
|
XM_005259617.3:c.1288G=
|
XP_005259674.1:p.Ala430=
|
|
XM_011528209.2:c.1066G=
|
XP_011526511.1:p.Ala356=
|
|
XR_001753738.2:n.2099G=
|
|
|
XR_001753740.2:n.2069G=
|
|
|
NM_000455.5:c.1293G=
MANE Select
|
NP_000446.1:p.Lys431=
|
|