ENST00000585465.3:c.*2847A>T
|
ENSP00000490268.2:n.*2847A>T
|
|
ENST00000585748.3:c.874A>T
|
ENSP00000477641.2:p.Lys292Ter
|
|
ENST00000585851.2:c.1072A>T
|
ENSP00000467912.2:p.Lys358Ter
|
|
ENST00000326873.12:c.1246A>T
MANE Select
|
ENSP00000324856.6:p.Lys416Ter
|
|
ENST00000326873.11:c.1246A>T
|
ENSP00000324856.6:p.Lys416Ter
|
|
ENST00000585465.2:n.2979A>T
|
|
|
ENST00000586243.5:c.1245A>T
|
ENSP00000467240.2:p.Ala415=
|
|
ENST00000589152.5:n.1944A>T
|
|
|
NM_000455.4:c.1246A>T , LRG_319t1:c.1246A>T
|
NP_000446.1:p.Lys416Ter
|
|
XM_005259617.1:c.1241A>T
|
XP_005259674.1:p.Gln414Leu
|
|
XM_011528209.1:c.1019A>T
|
XP_011526511.1:p.Gln340Leu
|
|
XM_005259617.3:c.1241A>T
|
XP_005259674.1:p.Gln414Leu
|
|
XM_011528209.2:c.1019A>T
|
XP_011526511.1:p.Gln340Leu
|
|
XR_001753738.2:n.2052A>T
|
|
|
XR_001753740.2:n.2022A>T
|
|
|
NM_000455.5:c.1246A>T
MANE Select
|
NP_000446.1:p.Lys416Ter
|
|