ENST00000585465.3:c.*2821A>C
|
ENSP00000490268.2:n.*2821A>C
|
|
ENST00000585748.3:c.848A>C
|
ENSP00000477641.2:p.Glu283Ala
|
|
ENST00000585851.2:c.1046A>C
|
ENSP00000467912.2:p.Glu349Ala
|
|
ENST00000326873.12:c.1220A>C
MANE Select
|
ENSP00000324856.6:p.Glu407Ala
|
|
ENST00000326873.11:c.1220A>C
|
ENSP00000324856.6:p.Glu407Ala
|
|
ENST00000585465.2:n.2953A>C
|
|
|
ENST00000586243.5:c.1220A>C
|
ENSP00000467240.2:p.Glu407Ala
|
|
ENST00000589152.5:n.1918A>C
|
|
|
NM_000455.4:c.1220A>C , LRG_319t1:c.1220A>C
|
NP_000446.1:p.Glu407Ala
|
|
XM_005259617.1:c.1215A>C
|
XP_005259674.1:p.Gly405=
|
|
XM_011528209.1:c.993A>C
|
XP_011526511.1:p.Gly331=
|
|
XM_005259617.3:c.1215A>C
|
XP_005259674.1:p.Gly405=
|
|
XM_011528209.2:c.993A>C
|
XP_011526511.1:p.Gly331=
|
|
XR_001753738.2:n.2026A>C
|
|
|
XR_001753740.2:n.1996A>C
|
|
|
NM_000455.5:c.1220A>C
MANE Select
|
NP_000446.1:p.Glu407Ala
|
|