ENST00000585465.3:c.*2801G=
|
ENSP00000490268.2:n.*2801G=
|
|
ENST00000585748.3:c.828G=
|
ENSP00000477641.2:p.Leu276=
|
|
ENST00000585851.2:c.1026G=
|
ENSP00000467912.2:p.Leu342=
|
|
ENST00000326873.12:c.1200G=
MANE Select
|
ENSP00000324856.6:p.Leu400=
|
|
ENST00000326873.11:c.1200G=
|
ENSP00000324856.6:p.Leu400=
|
|
ENST00000585465.2:n.2933G=
|
|
|
ENST00000586243.5:c.1200G=
|
ENSP00000467240.2:p.Leu400=
|
|
ENST00000589152.5:n.1898G=
|
|
|
NM_000455.4:c.1200G= , LRG_319t1:c.1200G=
|
NP_000446.1:p.Leu400=
|
|
XM_005259617.1:c.1195G=
|
XP_005259674.1:p.Glu399=
|
|
XM_011528209.1:c.973G=
|
XP_011526511.1:p.Glu325=
|
|
XM_005259617.3:c.1195G=
|
XP_005259674.1:p.Glu399=
|
|
XM_011528209.2:c.973G=
|
XP_011526511.1:p.Glu325=
|
|
XR_001753738.2:n.2006G=
|
|
|
XR_001753740.2:n.1976G=
|
|
|
NM_000455.5:c.1200G=
MANE Select
|
NP_000446.1:p.Leu400=
|
|