ENST00000264414.9:c.1215A>T
MANE Select
|
ENSP00000264414.4:p.Glu405Asp
|
|
ENST00000264414.8:c.1215A>T
|
ENSP00000264414.4:p.Glu405Asp
|
|
ENST00000344951.8:c.1017A>T
|
ENSP00000343601.4:p.Glu339Asp
|
|
ENST00000409096.5:c.1143A>T
|
ENSP00000387200.1:p.Glu381Asp
|
|
ENST00000409777.5:c.1143A>T
|
ENSP00000386525.1:p.Glu381Asp
|
|
ENST00000481135.1:n.511A>T
|
|
|
ENST00000617432.4:c.-62A>T
|
ENSP00000477851.1:n.-62A>T
|
|
NM_001257197.1:c.1017A>T
|
NP_001244126.1:p.Glu339Asp
|
|
NM_001257198.1:c.1233A>T
|
NP_001244127.1:p.Glu411Asp
|
|
NM_003590.4:c.1215A>T
|
NP_003581.1:p.Glu405Asp
|
|
XM_006712800.2:c.1182A>T
|
XP_006712863.2:p.Glu394Asp
|
|
XM_011511994.1:c.1068A>T
|
XP_011510296.1:p.Glu356Asp
|
|
XM_011511995.1:c.1173A>T
|
XP_011510297.1:p.Glu391Asp
|
|
XM_011511996.1:c.1023A>T
|
XP_011510298.1:p.Glu341Asp
|
|
XM_011511997.1:c.915A>T
|
XP_011510299.1:p.Glu305Asp
|
|
XM_011511994.3:c.1068A>T
|
XP_011510296.1:p.Glu356Asp
|
|
XM_011511996.2:c.1023A>T
|
XP_011510298.1:p.Glu341Asp
|
|
NM_003590.5:c.1215A>T
MANE Select
|
NP_003581.1:p.Glu405Asp
|
|
NM_001257198.2:c.1233A>T
|
NP_001244127.1:p.Glu411Asp
|
|
NM_001257197.2:c.1017A>T
|
NP_001244126.1:p.Glu339Asp
|
|