ENST00000356231.4:c.2133A>T
MANE Select
|
ENSP00000348564.3:p.Glu711Asp
|
|
ENST00000643434.1:c.*1311A>T
|
ENSP00000494699.1:n.*1311A>T
|
|
ENST00000356231.3:c.2133A>T
|
ENSP00000348564.3:p.Glu711Asp
|
|
ENST00000562465.5:c.126A>T
|
ENSP00000454246.1:p.Glu42Asp
|
|
NM_138477.2:c.2133A>T
|
NP_612486.2:p.Glu711Asp
|
|
XM_005254176.3:c.2136A>T
|
XP_005254233.1:p.Glu712Asp
|
|
XM_011521270.1:c.2160A>T
|
XP_011519572.1:p.Glu720Asp
|
|
XM_011521271.1:c.2157A>T
|
XP_011519573.1:p.Glu719Asp
|
|
XM_011521272.1:c.2160A>T
|
XP_011519574.1:p.Glu720Asp
|
|
XM_011521273.1:c.2160A>T
|
XP_011519575.1:p.Glu720Asp
|
|
XM_011521274.1:c.1125A>T
|
XP_011519576.1:p.Glu375Asp
|
|
XM_011521275.1:c.1377A>T
|
XP_011519577.1:p.Glu459Asp
|
|
XR_931757.1:n.2133A>T
|
|
|
NM_138477.4:c.2133A>T
MANE Select
|
NP_612486.2:p.Glu711Asp
|
|
XM_005254176.5:c.2136A>T
|
XP_005254233.1:p.Glu712Asp
|
|
XM_011521270.2:c.2160A>T
|
XP_011519572.1:p.Glu720Asp
|
|
XM_011521271.2:c.2157A>T
|
XP_011519573.1:p.Glu719Asp
|
|
XM_011521274.2:c.1125A>T
|
XP_011519576.1:p.Glu375Asp
|
|
XR_001751104.1:n.2190A>T
|
|
|
XR_001751105.1:n.2190A>T
|
|
|
XR_931757.2:n.2153A>T
|
|
|