ENST00000356518.7:c.1680G>T
MANE Select
|
ENSP00000348912.3:p.Glu560Asp
|
|
ENST00000350009.6:c.1680G>T
|
ENSP00000322550.5:p.Glu560Asp
|
|
ENST00000356518.6:c.1680G>T
|
ENSP00000348912.2:p.Glu560Asp
|
|
ENST00000379861.8:c.1680G>T
|
ENSP00000369190.4:p.Glu560Asp
|
|
ENST00000466620.5:n.1319G>T
|
|
|
ENST00000617732.1:c.*632-446G>T
|
ENSP00000483343.1:n.*632-446G>T
|
|
ENST00000619289.4:c.1320G>T
|
ENSP00000484600.1:p.Glu440Asp
|
|
NM_001282447.1:c.1680G>T
|
NP_001269376.1:p.Glu560Asp
|
|
NM_025220.3:c.1680G>T
|
NP_079496.1:p.Glu560Asp
|
|
NM_153202.2:c.1680G>T
|
NP_694882.1:p.Glu560Asp
|
|
XM_005260843.1:c.1719G>T
|
XP_005260900.1:p.Glu573Asp
|
|
XM_006723639.1:c.1719G>T
|
XP_006723702.1:p.Glu573Asp
|
|
XM_006723640.1:c.1710G>T
|
XP_006723703.1:p.Glu570Asp
|
|
XM_011529366.1:c.1716G>T
|
XP_011527668.1:p.Glu572Asp
|
|
XM_011529367.1:c.1677G>T
|
XP_011527669.1:p.Glu559Asp
|
|
XM_011529368.1:c.1719G>T
|
XP_011527670.1:p.Glu573Asp
|
|
XM_011529369.1:c.1687G>T
|
XP_011527671.1:p.Gly563Trp
|
|
XM_011529370.1:c.1687G>T
|
XP_011527672.1:p.Gly563Trp
|
|
XM_011529373.1:c.717G>T
|
XP_011527675.1:p.Glu239Asp
|
|
XR_937151.1:n.1823G>T
|
|
|
XR_937152.1:n.1823G>T
|
|
|
XR_937153.1:n.1704G>T
|
|
|
XR_937154.1:n.1704G>T
|
|
|
XR_937155.1:n.1625G>T
|
|
|
XR_937157.1:n.1627G>T
|
|
|
NM_001282447.2:c.1680G>T
|
NP_001269376.1:p.Glu560Asp
|
|
NM_025220.4:c.1680G>T
|
NP_079496.1:p.Glu560Asp
|
|
NM_153202.3:c.1680G>T
|
NP_694882.1:p.Glu560Asp
|
|
XM_011529373.2:c.717G>T
|
XP_011527675.1:p.Glu239Asp
|
|
XR_001754405.1:n.1791G>T
|
|
|
XR_002958534.1:n.1900G>T
|
|
|
NM_001282447.3:c.1680G>T
|
NP_001269376.1:p.Glu560Asp
|
|
NM_025220.5:c.1680G>T
MANE Select
|
NP_079496.1:p.Glu560Asp
|
|
NM_153202.4:c.1680G>T
|
NP_694882.1:p.Glu560Asp
|
|