ENST00000585465.3:c.*2712C=
|
ENSP00000490268.2:n.*2712C=
|
|
ENST00000585748.3:c.739C=
|
ENSP00000477641.2:p.Gln247=
|
|
ENST00000585851.2:c.937C=
|
ENSP00000467912.2:p.Gln313=
|
|
ENST00000326873.12:c.1111C=
MANE Select
|
ENSP00000324856.6:p.Gln371=
|
|
ENST00000326873.11:c.1111C=
|
ENSP00000324856.6:p.Gln371=
|
|
ENST00000585465.2:n.2844C=
|
|
|
ENST00000586243.5:c.1111C=
|
ENSP00000467240.2:p.Gln371=
|
|
ENST00000589152.5:n.1809C=
|
|
|
NM_000455.4:c.1111C= , LRG_319t1:c.1111C=
|
NP_000446.1:p.Gln371=
|
|
XM_005259617.1:c.1109-3C=
|
XP_005259674.1:n.1109-3C=
|
|
XM_011528209.1:c.887-3C=
|
XP_011526511.1:n.887-3C=
|
|
XM_005259617.3:c.1109-3C=
|
XP_005259674.1:n.1109-3C=
|
|
XM_011528209.2:c.887-3C=
|
XP_011526511.1:n.887-3C=
|
|
XR_001753738.2:n.1917C=
|
|
|
XR_001753740.2:n.1887C=
|
|
|
NM_000455.5:c.1111C=
MANE Select
|
NP_000446.1:p.Gln371=
|
|