ENST00000223073.6:c.1041A>C
MANE Select
|
ENSP00000223073.1:p.Glu347Asp
|
|
ENST00000415472.6:c.618A>C
|
ENSP00000390517.2:p.Glu206Asp
|
|
ENST00000487602.5:c.458A>C
|
|
|
NM_001166135.1:c.618A>C
|
NP_001159607.1:p.Glu206Asp
|
|
NM_018077.2:c.1041A>C
|
NP_060547.2:p.Glu347Asp
|
|
XM_011516370.1:c.1143A>C
|
XP_011514672.1:p.Glu381Asp
|
|
XM_011516371.1:c.47A>C
|
XP_011514673.1:p.Lys16Thr
|
|
XR_927487.1:n.1263A>C
|
|
|
XM_011516370.3:c.1143A>C
|
XP_011514672.1:p.Glu381Asp
|
|
XM_017012389.1:c.1143A>C
|
XP_016867878.1:p.Glu381Asp
|
|
XM_017012390.1:c.1041A>C
|
XP_016867879.1:p.Glu347Asp
|
|
XR_001744830.1:n.1265A>C
|
|
|
NM_001166135.2:c.618A>C
|
NP_001159607.1:p.Glu206Asp
|
|
NM_018077.3:c.1041A>C
MANE Select
|
NP_060547.2:p.Glu347Asp
|
|