ENST00000205402.10:c.768G>A
MANE Select
|
ENSP00000205402.3:p.Glu256=
|
|
ENST00000205402.9:c.768G>A
|
ENSP00000205402.3:p.Glu256=
|
|
ENST00000415325.5:c.*442G>A
|
ENSP00000402593.1:n.*442G>A
|
|
ENST00000417551.5:c.768G>A
|
ENSP00000390667.1:p.Glu256=
|
|
ENST00000437604.6:c.624G>A
|
ENSP00000387542.2:p.Glu208=
|
|
ENST00000440410.5:c.699G>A
|
ENSP00000417016.1:p.Glu233=
|
|
ENST00000451081.5:c.*511G>A
|
ENSP00000388077.1:n.*511G>A
|
|
NM_000108.4:c.768G>A
|
NP_000099.2:p.Glu256=
|
|
NM_001289750.1:c.471G>A
|
NP_001276679.1:p.Glu157=
|
|
NM_001289751.1:c.699G>A
|
NP_001276680.1:p.Glu233=
|
|
NM_001289752.1:c.624G>A
|
NP_001276681.1:p.Glu208=
|
|
NM_000108.5:c.768G>A
MANE Select
|
NP_000099.2:p.Glu256=
|
|