ENST00000368666.7:c.1029A>T
MANE Select
|
ENSP00000357655.4:p.Glu343Asp
|
|
ENST00000639360.1:c.930A>T
|
ENSP00000491774.1:p.Glu310Asp
|
|
ENST00000230529.9:c.1029A>T
|
ENSP00000230529.5:p.Glu343Asp
|
|
ENST00000361714.5:c.1029A>T
|
ENSP00000354734.2:p.Glu343Asp
|
|
ENST00000368663.4:c.*335A>T
|
ENSP00000357652.4:n.*335A>T
|
|
ENST00000368664.7:c.*433A>T
|
ENSP00000357653.3:n.*433A>T
|
|
ENST00000368666.6:c.1083A>T
|
ENSP00000357655.3:p.Glu361Asp
|
|
ENST00000409166.5:c.357A>T
|
ENSP00000386467.1:p.Glu119Asp
|
|
ENST00000454589.5:c.*433A>T
|
ENSP00000395928.1:n.*433A>T
|
|
ENST00000604763.5:c.1029A>T
|
ENSP00000473777.1:p.Glu343Asp
|
|
ENST00000613648.1:n.864A>T
|
|
|
ENST00000620524.3:n.960A>T
|
|
|
NM_003880.3:c.1029A>T
|
NP_003871.1:p.Glu343Asp
|
|
NM_198239.1:c.1083A>T
|
NP_937882.1:p.Glu361Asp
|
|
NR_125353.1:n.1283A>T
|
|
|
NR_125354.1:n.1203A>T
|
|
|
XM_011536220.1:c.1029A>T
|
XP_011534522.1:p.Glu343Asp
|
|
XM_011536221.1:c.*433A>T
|
XP_011534523.1:n.*433A>T
|
|
XM_011536223.1:c.447A>T
|
XP_011534525.1:p.Glu149Asp
|
|
XM_011536223.3:c.447A>T
|
XP_011534525.1:p.Glu149Asp
|
|
XR_001743705.1:n.1631A>T
|
|
|
NM_003880.4:c.1029A>T
|
NP_003871.1:p.Glu343Asp
|
|
NM_198239.2:c.1029A>T
MANE Select
|
NP_937882.2:p.Glu343Asp
|
|
NR_125353.2:n.1347A>T
|
|
|
NR_125354.3:n.1174A>T
|
|
|