ENST00000295897.9:c.1556A>T
MANE Select
|
ENSP00000295897.4:p.Glu519Val
|
|
ENST00000295897.8:c.1556A>T
|
ENSP00000295897.4:p.Glu519Val
|
|
ENST00000401494.7:c.1211A>T
|
ENSP00000384695.3:p.Glu404Val
|
|
ENST00000415165.6:c.980A>T
|
ENSP00000401820.2:p.Glu327Val
|
|
ENST00000476441.6:c.*835A>T
|
ENSP00000423727.1:n.*835A>T
|
|
ENST00000486939.1:n.210A>T
|
|
|
ENST00000503124.5:c.1106A>T
|
ENSP00000421027.1:p.Glu369Val
|
|
ENST00000505649.5:n.1103A>T
|
|
|
ENST00000509063.5:c.1556A>T
|
ENSP00000422784.1:p.Glu519Val
|
|
ENST00000511370.1:c.1089A>T
|
|
|
ENST00000621085.4:c.917A>T
|
ENSP00000483421.1:p.Glu306Val
|
|
ENST00000621628.4:c.917A>T
|
ENSP00000480485.1:p.Glu306Val
|
|
NM_000477.5:c.1556A>T
|
NP_000468.1:p.Glu519Val
|
|
NM_000477.6:c.1556A>T
|
NP_000468.1:p.Glu519Val
|
|
NM_000477.7:c.1556A>T
MANE Select
|
NP_000468.1:p.Glu519Val
|
|