ENST00000585465.3:c.*2813C>G
|
ENSP00000490268.2:n.*2813C>G
|
|
ENST00000585748.3:c.840C>G
|
ENSP00000477641.2:p.Ser280=
|
|
ENST00000585851.2:c.1038C>G
|
ENSP00000467912.2:p.Ser346=
|
|
ENST00000326873.12:c.1212C>G
MANE Select
|
ENSP00000324856.6:p.Ser404=
|
|
ENST00000326873.11:c.1212C>G
|
ENSP00000324856.6:p.Ser404=
|
|
ENST00000585465.2:n.2945C>G
|
|
|
ENST00000586243.5:c.1212C>G
|
ENSP00000467240.2:p.Ser404=
|
|
ENST00000589152.5:n.1910C>G
|
|
|
NM_000455.4:c.1212C>G , LRG_319t1:c.1212C>G
|
NP_000446.1:p.Ser404=
|
|
XM_005259617.1:c.1207C>G
|
XP_005259674.1:p.Gln403Glu
|
|
XM_011528209.1:c.985C>G
|
XP_011526511.1:p.Gln329Glu
|
|
XM_005259617.3:c.1207C>G
|
XP_005259674.1:p.Gln403Glu
|
|
XM_011528209.2:c.985C>G
|
XP_011526511.1:p.Gln329Glu
|
|
XR_001753738.2:n.2018C>G
|
|
|
XR_001753740.2:n.1988C>G
|
|
|
NM_000455.5:c.1212C>G
MANE Select
|
NP_000446.1:p.Ser404=
|
|