ENST00000357578.8:c.1290G=
MANE Select
|
ENSP00000350191.3:p.Gln430=
|
|
ENST00000479394.2:n.405G=
|
|
|
ENST00000672352.1:c.909G=
|
ENSP00000500876.1:p.Gln303=
|
|
ENST00000672652.1:c.1253G=
|
|
|
ENST00000348925.2:c.1329G=
|
ENSP00000314649.3:p.Gln443=
|
|
ENST00000357578.7:c.1290G=
|
ENSP00000350191.3:p.Gln430=
|
|
ENST00000479394.1:n.405G=
|
|
|
ENST00000491546.5:c.1206G=
|
ENSP00000417687.1:p.Gln402=
|
|
NM_001080.3:c.1290G=
MANE Select
|
NP_001071.1:p.Gln430=
|
|
NM_170740.1:c.1329G=
|
NP_733936.1:p.Gln443=
|
|
NM_001368954.1:c.1146G=
|
NP_001355883.1:p.Gln382=
|
|