ENST00000585465.3:c.*2888C>G
|
ENSP00000490268.2:n.*2888C>G
|
|
ENST00000585748.3:c.915C>G
|
ENSP00000477641.2:p.Ala305=
|
|
ENST00000585851.2:c.1113C>G
|
ENSP00000467912.2:p.Ala371=
|
|
ENST00000326873.12:c.1287C>G
MANE Select
|
ENSP00000324856.6:p.Ala429=
|
|
ENST00000326873.11:c.1287C>G
|
ENSP00000324856.6:p.Ala429=
|
|
ENST00000585465.2:n.3020C>G
|
|
|
ENST00000586243.5:c.1284C>G
|
ENSP00000467240.2:p.Ala428=
|
|
ENST00000589152.5:n.1985C>G
|
|
|
NM_000455.4:c.1287C>G , LRG_319t1:c.1287C>G
|
NP_000446.1:p.Ala429=
|
|
XM_005259617.1:c.1282C>G
|
XP_005259674.1:p.Leu428Val
|
|
XM_011528209.1:c.1060C>G
|
XP_011526511.1:p.Leu354Val
|
|
XM_005259617.3:c.1282C>G
|
XP_005259674.1:p.Leu428Val
|
|
XM_011528209.2:c.1060C>G
|
XP_011526511.1:p.Leu354Val
|
|
XR_001753738.2:n.2093C>G
|
|
|
XR_001753740.2:n.2063C>G
|
|
|
NM_000455.5:c.1287C>G
MANE Select
|
NP_000446.1:p.Ala429=
|
|