ENST00000706952.1:c.3147G>T
|
ENSP00000516672.1:p.Glu1049Asp
|
|
ENST00000638521.1:c.940G>T
|
|
|
ENST00000638869.1:c.449G>T
|
|
|
ENST00000639642.1:c.278G>T
|
|
|
ENST00000640005.1:c.51G>T
|
ENSP00000491293.1:p.Glu17Asp
|
|
ENST00000640694.1:c.2988G>T
|
ENSP00000492403.1:p.Glu996Asp
|
|
ENST00000642864.1:c.2988G>T
MANE Select
|
ENSP00000495726.1:p.Glu996Asp
|
|
ENST00000674510.1:c.2988G>T
|
ENSP00000502054.1:p.Glu996Asp
|
|
ENST00000674761.1:n.1295G>T
|
|
|
ENST00000675719.1:c.2958G>T
|
ENSP00000501927.1:p.Glu986Asp
|
|
ENST00000375365.2:c.2373G>T
|
ENSP00000364514.2:p.Glu791Asp
|
|
ENST00000396435.7:c.2988G>T
|
ENSP00000379712.3:p.Glu996Asp
|
|
NM_001111125.2:c.2988G>T
|
NP_001104595.1:p.Glu996Asp
|
|
NM_015075.1:c.2373G>T
|
NP_055890.1:p.Glu791Asp
|
|
XM_006724579.2:c.3084G>T
|
XP_006724642.1:p.Glu1028Asp
|
|
XM_006724580.2:c.2373G>T
|
XP_006724643.1:p.Glu791Asp
|
|
XM_006724581.2:c.3084G>T
|
XP_006724644.1:p.Glu1028Asp
|
|
XM_006724582.2:c.3084G>T
|
XP_006724645.1:p.Glu1028Asp
|
|
XM_006724583.2:c.3084G>T
|
XP_006724646.1:p.Glu1028Asp
|
|
XM_006724584.2:c.3084G>T
|
XP_006724647.1:p.Glu1028Asp
|
|
XM_011530772.1:c.2310G>T
|
XP_011529074.1:p.Glu770Asp
|
|
XM_011530773.1:c.2277G>T
|
XP_011529075.1:p.Glu759Asp
|
|
XM_011530774.1:c.3084G>T
|
XP_011529076.1:p.Glu1028Asp
|
|
XM_011530775.1:c.3084G>T
|
XP_011529077.1:p.Glu1028Asp
|
|
XM_011530776.1:c.3084G>T
|
XP_011529078.1:p.Glu1028Asp
|
|
XM_011530777.1:c.3084G>T
|
XP_011529079.1:p.Glu1028Asp
|
|
XR_938365.1:n.3311G>T
|
|
|
XM_006724579.3:c.3084G>T
|
XP_006724642.1:p.Glu1028Asp
|
|
XM_006724580.3:c.2373G>T
|
XP_006724643.1:p.Glu791Asp
|
|
XM_006724581.4:c.3084G>T
|
XP_006724644.1:p.Glu1028Asp
|
|
XM_006724582.4:c.3084G>T
|
XP_006724645.1:p.Glu1028Asp
|
|
XM_006724583.4:c.3084G>T
|
XP_006724646.1:p.Glu1028Asp
|
|
XM_006724584.3:c.3084G>T
|
XP_006724647.1:p.Glu1028Asp
|
|
XM_011530773.2:c.2277G>T
|
XP_011529075.1:p.Glu759Asp
|
|
XM_011530774.3:c.3084G>T
|
XP_011529076.1:p.Glu1028Asp
|
|
XM_011530776.2:c.3084G>T
|
XP_011529078.1:p.Glu1028Asp
|
|
XM_011530777.2:c.3084G>T
|
XP_011529079.1:p.Glu1028Asp
|
|
XM_017029359.2:c.2958G>T
|
XP_016884848.1:p.Glu986Asp
|
|
XM_017029360.1:c.2490G>T
|
XP_016884849.1:p.Glu830Asp
|
|
XR_938365.2:n.3305G>T
|
|
|
NM_001111125.3:c.2988G>T
MANE Select
|
NP_001104595.1:p.Glu996Asp
|
|
NM_015075.2:c.2373G>T
|
NP_055890.1:p.Glu791Asp
|
|