ENST00000700029.2:c.1212A>C
|
ENSP00000514759.2:p.Glu404Asp
|
|
ENST00000710265.1:c.*148A>C
|
ENSP00000518161.1:n.*148A>C
|
|
ENST00000688158.2:n.1854A>C
|
|
|
ENST00000688922.2:c.*949A>C
|
ENSP00000508742.2:n.*949A>C
|
|
ENST00000700021.1:c.1074A>C
|
ENSP00000514757.1:p.Glu358Asp
|
|
ENST00000700022.1:c.*458A>C
|
ENSP00000514758.1:n.*458A>C
|
|
ENST00000700023.1:n.2277A>C
|
|
|
ENST00000700024.1:n.2511A>C
|
|
|
ENST00000706954.1:c.1119A>C
|
ENSP00000516674.1:p.Glu373Asp
|
|
ENST00000706955.1:c.*1154A>C
|
ENSP00000516675.1:n.*1154A>C
|
|
ENST00000686459.1:c.*705A>C
|
ENSP00000508909.1:n.*705A>C
|
|
ENST00000688158.1:c.*1230A>C
|
ENSP00000509254.1:n.*1230A>C
|
|
ENST00000688308.1:c.1119A>C
|
ENSP00000508752.1:p.Glu373Asp
|
|
ENST00000688922.1:c.1040A>C
|
|
|
ENST00000693560.1:c.1638A>C
|
ENSP00000509861.1:p.Glu546Asp
|
|
ENST00000371953.8:c.1119A>C
MANE Select
|
ENSP00000361021.3:p.Glu373Asp
|
|
ENST00000371953.7:c.1119A>C
|
ENSP00000361021.3:p.Glu373Asp
|
|
NM_000314.5:c.1119A>C
|
NP_000305.3:p.Glu373Asp
|
|
NM_000314.6:c.1119A>C
|
NP_000305.3:p.Glu373Asp
|
|
NM_001304717.2:c.1638A>C
|
NP_001291646.2:p.Glu546Asp
|
|
NM_001304718.1:c.528A>C
|
NP_001291647.1:p.Glu176Asp
|
|
XM_006717926.2:c.1074A>C
|
XP_006717989.1:p.Glu358Asp
|
|
XM_011539982.1:c.1023A>C
|
XP_011538284.1:p.Glu341Asp
|
|
XR_945791.1:n.1689A>C
|
|
|
NM_000314.7:c.1119A>C
|
NP_000305.3:p.Glu373Asp
|
|
NM_001304717.5:c.1638A>C
|
NP_001291646.4:p.Glu546Asp
|
|
NM_001304718.2:c.528A>C
|
NP_001291647.1:p.Glu176Asp
|
|
NM_000314.8:c.1119A>C
MANE Select
|
NP_000305.3:p.Glu373Asp
|
|