ENST00000295897.9:c.1175A>T
MANE Select
|
ENSP00000295897.4:p.Glu392Val
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|
ENST00000295897.8:c.1175A>T
|
ENSP00000295897.4:p.Glu392Val
|
|
ENST00000401494.7:c.830A>T
|
ENSP00000384695.3:p.Glu277Val
|
|
ENST00000415165.6:c.599A>T
|
ENSP00000401820.2:p.Glu200Val
|
|
ENST00000476441.6:c.*454A>T
|
ENSP00000423727.1:n.*454A>T
|
|
ENST00000484992.1:n.495A>T
|
|
|
ENST00000503124.5:c.725A>T
|
ENSP00000421027.1:p.Glu242Val
|
|
ENST00000504043.1:n.178A>T
|
|
|
ENST00000505649.5:n.861A>T
|
|
|
ENST00000509063.5:c.1175A>T
|
ENSP00000422784.1:p.Glu392Val
|
|
ENST00000511370.1:c.708A>T
|
|
|
ENST00000621085.4:c.536A>T
|
ENSP00000483421.1:p.Glu179Val
|
|
ENST00000621628.4:c.536A>T
|
ENSP00000480485.1:p.Glu179Val
|
|
NM_000477.5:c.1175A>T
|
NP_000468.1:p.Glu392Val
|
|
NM_000477.6:c.1175A>T
|
NP_000468.1:p.Glu392Val
|
|
NM_000477.7:c.1175A>T
MANE Select
|
NP_000468.1:p.Glu392Val
|
|