ENST00000356231.4:c.2131G>A
MANE Select
|
ENSP00000348564.3:p.Glu711Lys
|
|
ENST00000643434.1:c.*1309G>A
|
ENSP00000494699.1:n.*1309G>A
|
|
ENST00000356231.3:c.2131G>A
|
ENSP00000348564.3:p.Glu711Lys
|
|
ENST00000562465.5:c.124G>A
|
ENSP00000454246.1:p.Glu42Lys
|
|
NM_138477.2:c.2131G>A
|
NP_612486.2:p.Glu711Lys
|
|
XM_005254176.3:c.2134G>A
|
XP_005254233.1:p.Glu712Lys
|
|
XM_011521270.1:c.2158G>A
|
XP_011519572.1:p.Glu720Lys
|
|
XM_011521271.1:c.2155G>A
|
XP_011519573.1:p.Glu719Lys
|
|
XM_011521272.1:c.2158G>A
|
XP_011519574.1:p.Glu720Lys
|
|
XM_011521273.1:c.2158G>A
|
XP_011519575.1:p.Glu720Lys
|
|
XM_011521274.1:c.1123G>A
|
XP_011519576.1:p.Glu375Lys
|
|
XM_011521275.1:c.1375G>A
|
XP_011519577.1:p.Glu459Lys
|
|
XR_931757.1:n.2131G>A
|
|
|
NM_138477.4:c.2131G>A
MANE Select
|
NP_612486.2:p.Glu711Lys
|
|
XM_005254176.5:c.2134G>A
|
XP_005254233.1:p.Glu712Lys
|
|
XM_011521270.2:c.2158G>A
|
XP_011519572.1:p.Glu720Lys
|
|
XM_011521271.2:c.2155G>A
|
XP_011519573.1:p.Glu719Lys
|
|
XM_011521274.2:c.1123G>A
|
XP_011519576.1:p.Glu375Lys
|
|
XR_001751104.1:n.2188G>A
|
|
|
XR_001751105.1:n.2188G>A
|
|
|
XR_931757.2:n.2151G>A
|
|
|