ENST00000585465.3:c.*2788A>T
|
ENSP00000490268.2:n.*2788A>T
|
|
ENST00000585748.3:c.815A>T
|
ENSP00000477641.2:p.Glu272Val
|
|
ENST00000585851.2:c.1013A>T
|
ENSP00000467912.2:p.Glu338Val
|
|
ENST00000326873.12:c.1187A>T
MANE Select
|
ENSP00000324856.6:p.Glu396Val
|
|
ENST00000326873.11:c.1187A>T
|
ENSP00000324856.6:p.Glu396Val
|
|
ENST00000585465.2:n.2920A>T
|
|
|
ENST00000586243.5:c.1187A>T
|
ENSP00000467240.2:p.Glu396Val
|
|
ENST00000589152.5:n.1885A>T
|
|
|
NM_000455.4:c.1187A>T , LRG_319t1:c.1187A>T
|
NP_000446.1:p.Glu396Val
|
|
XM_005259617.1:c.1182A>T
|
XP_005259674.1:p.Arg394Ser
|
|
XM_011528209.1:c.960A>T
|
XP_011526511.1:p.Arg320Ser
|
|
XM_005259617.3:c.1182A>T
|
XP_005259674.1:p.Arg394Ser
|
|
XM_011528209.2:c.960A>T
|
XP_011526511.1:p.Arg320Ser
|
|
XR_001753738.2:n.1993A>T
|
|
|
XR_001753740.2:n.1963A>T
|
|
|
NM_000455.5:c.1187A>T
MANE Select
|
NP_000446.1:p.Glu396Val
|
|