ENST00000297784.10:c.1175A>T
MANE Select
|
ENSP00000297784.6:p.Glu392Val
|
|
ENST00000644967.1:c.737A>T
|
ENSP00000496159.1:p.Glu246Val
|
|
ENST00000645053.1:c.737A>T
|
ENSP00000493838.1:p.Glu246Val
|
|
ENST00000645208.2:c.1175A>T
|
ENSP00000494684.1:p.Glu392Val
|
|
ENST00000645773.1:c.1049A>T
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ENSP00000493698.1:p.Glu350Val
|
|
ENST00000645787.1:n.1215A>T
|
|
|
ENST00000646619.1:c.737A>T
|
ENSP00000493726.1:p.Glu246Val
|
|
ENST00000650689.1:n.1473A>T
|
|
|
ENST00000651183.1:c.737A>T
|
ENSP00000498723.1:p.Glu246Val
|
|
ENST00000297784.9:c.1175A>T
|
ENSP00000297784.5:p.Glu392Val
|
|
ENST00000340019.4:c.1175A>T
|
ENSP00000341433.3:p.Glu392Val
|
|
NM_138691.2:c.1175A>T
|
NP_619636.2:p.Glu392Val
|
|
XM_011518213.1:c.1763A>T
|
XP_011516515.1:p.Glu588Val
|
|
XM_017014256.1:c.1178A>T
|
XP_016869745.1:p.Glu393Val
|
|
NM_138691.3:c.1175A>T
MANE Select
|
NP_619636.2:p.Glu392Val
|
|