ENST00000585465.3:c.*2846C>G
|
ENSP00000490268.2:n.*2846C>G
|
|
ENST00000585748.3:c.873C>G
|
ENSP00000477641.2:p.Arg291=
|
|
ENST00000585851.2:c.1071C>G
|
ENSP00000467912.2:p.Arg357=
|
|
ENST00000326873.12:c.1245C>G
MANE Select
|
ENSP00000324856.6:p.Arg415=
|
|
ENST00000326873.11:c.1245C>G
|
ENSP00000324856.6:p.Arg415=
|
|
ENST00000585465.2:n.2978C>G
|
|
|
ENST00000586243.5:c.1244C>G
|
ENSP00000467240.2:p.Ala415Gly
|
|
ENST00000589152.5:n.1943C>G
|
|
|
NM_000455.4:c.1245C>G , LRG_319t1:c.1245C>G
|
NP_000446.1:p.Arg415=
|
|
XM_005259617.1:c.1240C>G
|
XP_005259674.1:p.Gln414Glu
|
|
XM_011528209.1:c.1018C>G
|
XP_011526511.1:p.Gln340Glu
|
|
XM_005259617.3:c.1240C>G
|
XP_005259674.1:p.Gln414Glu
|
|
XM_011528209.2:c.1018C>G
|
XP_011526511.1:p.Gln340Glu
|
|
XR_001753738.2:n.2051C>G
|
|
|
XR_001753740.2:n.2021C>G
|
|
|
NM_000455.5:c.1245C>G
MANE Select
|
NP_000446.1:p.Arg415=
|
|