ENST00000369538.4:c.1277G>T
|
ENSP00000358551.4:p.Gly426Val
|
|
ENST00000520113.7:c.1289G>T
MANE Select
|
ENSP00000430075.3:p.Gly430Val
|
|
ENST00000637080.1:c.1072G>T
|
ENSP00000489753.1:n.1072G>T
|
|
ENST00000639077.1:n.954G>T
|
|
|
ENST00000369538.3:c.1376G>T
|
ENSP00000358551.3:p.Gly459Val
|
|
ENST00000520113.6:c.1388G>T
|
ENSP00000430075.2:p.Gly463Val
|
|
NM_000036.2:c.1388G>T
|
NP_000027.2:p.Gly463Val
|
|
NM_001172626.1:c.1376G>T
|
NP_001166097.1:p.Gly459Val
|
|
NM_000036.3:c.1289G>T
MANE Select
|
NP_000027.3:p.Gly430Val
|
|
NM_001172626.2:c.1277G>T
|
NP_001166097.2:p.Gly426Val
|
|