ENST00000253122.10:c.1204T>A
MANE Select
|
ENSP00000253122.5:p.Trp402Arg
|
|
ENST00000253122.9:c.1204T>A
|
ENSP00000253122.5:p.Trp402Arg
|
|
ENST00000413787.1:c.258-237T>A
|
ENSP00000400463.1:n.258-237T>A
|
|
ENST00000430077.6:c.859T>A
|
ENSP00000403041.2:p.Trp287Arg
|
|
ENST00000442457.1:c.258T>A
|
|
|
ENST00000457723.1:c.188T>A
|
ENSP00000394742.1:p.Leu63Gln
|
|
ENST00000467402.1:n.303T>A
|
|
|
ENST00000485324.1:n.1237T>A
|
|
|
NM_001142805.1:c.1174T>A
|
NP_001136277.1:p.Trp392Arg
|
|
NM_001142806.1:c.859T>A
|
NP_001136278.1:p.Trp287Arg
|
|
NM_005629.3:c.1204T>A
|
NP_005620.1:p.Trp402Arg
|
|
NM_005629.4:c.1204T>A
MANE Select
|
NP_005620.1:p.Trp402Arg
|
|
NM_001142805.2:c.1174T>A
|
NP_001136277.1:p.Trp392Arg
|
|