ENST00000585465.3:c.*2774T=
|
ENSP00000490268.2:n.*2774T=
|
|
ENST00000585748.3:c.801T=
|
ENSP00000477641.2:p.Cys267=
|
|
ENST00000585851.2:c.999T=
|
ENSP00000467912.2:p.Cys333=
|
|
ENST00000326873.12:c.1173T=
MANE Select
|
ENSP00000324856.6:p.Cys391=
|
|
ENST00000326873.11:c.1173T=
|
ENSP00000324856.6:p.Cys391=
|
|
ENST00000585465.2:n.2906T=
|
|
|
ENST00000586243.5:c.1173T=
|
ENSP00000467240.2:p.Cys391=
|
|
ENST00000589152.5:n.1871T=
|
|
|
NM_000455.4:c.1173T= , LRG_319t1:c.1173T=
|
NP_000446.1:p.Cys391=
|
|
XM_005259617.1:c.1168T=
|
XP_005259674.1:p.Tyr390=
|
|
XM_011528209.1:c.946T=
|
XP_011526511.1:p.Tyr316=
|
|
XM_005259617.3:c.1168T=
|
XP_005259674.1:p.Tyr390=
|
|
XM_011528209.2:c.946T=
|
XP_011526511.1:p.Tyr316=
|
|
XR_001753738.2:n.1979T=
|
|
|
XR_001753740.2:n.1949T=
|
|
|
NM_000455.5:c.1173T=
MANE Select
|
NP_000446.1:p.Cys391=
|
|