ENST00000336906.6:c.377A>T
MANE Select
|
ENSP00000338082.4:p.Glu126Val
|
|
ENST00000380252.6:c.212A>T
|
ENSP00000369602.2:p.Glu71Val
|
|
ENST00000642908.1:c.315+948A>T
|
ENSP00000495346.1:n.315+948A>T
|
|
ENST00000647543.1:c.377A>T
|
ENSP00000496470.1:p.Glu126Val
|
|
ENST00000336906.4:c.377A>T
|
ENSP00000338082.4:p.Glu126Val
|
|
ENST00000380252.5:c.347A>T
|
ENSP00000369602.1:p.Glu116Val
|
|
ENST00000380259.6:c.377A>T
|
ENSP00000369609.2:p.Glu126Val
|
|
ENST00000620888.4:c.315+948A>T
|
ENSP00000479637.1:n.315+948A>T
|
|
NM_000184.2:c.377A>T
|
NP_000175.1:p.Glu126Val
|
|
NM_000184.3:c.377A>T
MANE Select
|
NP_000175.1:p.Glu126Val
|
|