ENST00000253122.10:c.1331A>T
MANE Select
|
ENSP00000253122.5:p.Glu444Val
|
|
ENST00000253122.9:c.1331A>T
|
ENSP00000253122.5:p.Glu444Val
|
|
ENST00000413787.1:c.260A>T
|
ENSP00000400463.1:p.Glu87Val
|
|
ENST00000430077.6:c.986A>T
|
ENSP00000403041.2:p.Glu329Val
|
|
ENST00000442457.1:c.385A>T
|
|
|
ENST00000485324.1:n.1476A>T
|
|
|
NM_001142805.1:c.1301A>T
|
NP_001136277.1:p.Glu434Val
|
|
NM_001142806.1:c.986A>T
|
NP_001136278.1:p.Glu329Val
|
|
NM_005629.3:c.1331A>T
|
NP_005620.1:p.Glu444Val
|
|
NM_005629.4:c.1331A>T
MANE Select
|
NP_005620.1:p.Glu444Val
|
|
NM_001142805.2:c.1301A>T
|
NP_001136277.1:p.Glu434Val
|
|