ENST00000585465.3:c.*2800T=
|
ENSP00000490268.2:n.*2800T=
|
|
ENST00000585748.3:c.827T=
|
ENSP00000477641.2:p.Leu276=
|
|
ENST00000585851.2:c.1025T=
|
ENSP00000467912.2:p.Leu342=
|
|
ENST00000326873.12:c.1199T=
MANE Select
|
ENSP00000324856.6:p.Leu400=
|
|
ENST00000326873.11:c.1199T=
|
ENSP00000324856.6:p.Leu400=
|
|
ENST00000585465.2:n.2932T=
|
|
|
ENST00000586243.5:c.1199T=
|
ENSP00000467240.2:p.Leu400=
|
|
ENST00000589152.5:n.1897T=
|
|
|
NM_000455.4:c.1199T= , LRG_319t1:c.1199T=
|
NP_000446.1:p.Leu400=
|
|
XM_005259617.1:c.1194T=
|
XP_005259674.1:p.Ala398=
|
|
XM_011528209.1:c.972T=
|
XP_011526511.1:p.Ala324=
|
|
XM_005259617.3:c.1194T=
|
XP_005259674.1:p.Ala398=
|
|
XM_011528209.2:c.972T=
|
XP_011526511.1:p.Ala324=
|
|
XR_001753738.2:n.2005T=
|
|
|
XR_001753740.2:n.1975T=
|
|
|
NM_000455.5:c.1199T=
MANE Select
|
NP_000446.1:p.Leu400=
|
|