ENST00000357578.8:c.1314G=
MANE Select
|
ENSP00000350191.3:p.Glu438=
|
|
ENST00000479394.2:n.429G=
|
|
|
ENST00000672352.1:c.933G=
|
ENSP00000500876.1:p.Glu311=
|
|
ENST00000672652.1:c.1277G=
|
|
|
ENST00000348925.2:c.1353G=
|
ENSP00000314649.3:p.Glu451=
|
|
ENST00000357578.7:c.1314G=
|
ENSP00000350191.3:p.Glu438=
|
|
ENST00000479394.1:n.429G=
|
|
|
ENST00000491546.5:c.1230G=
|
ENSP00000417687.1:p.Glu410=
|
|
NM_001080.3:c.1314G=
MANE Select
|
NP_001071.1:p.Glu438=
|
|
NM_170740.1:c.1353G=
|
NP_733936.1:p.Glu451=
|
|
NM_001368954.1:c.1170G=
|
NP_001355883.1:p.Glu390=
|
|