ENST00000356518.7:c.1708G>T
MANE Select
|
ENSP00000348912.3:p.Asp570Tyr
|
|
ENST00000350009.6:c.1708G>T
|
ENSP00000322550.5:p.Asp570Tyr
|
|
ENST00000356518.6:c.1708G>T
|
ENSP00000348912.2:p.Asp570Tyr
|
|
ENST00000379861.8:c.1708G>T
|
ENSP00000369190.4:p.Asp570Tyr
|
|
ENST00000466620.5:n.1347G>T
|
|
|
ENST00000617732.1:c.*632-321G>T
|
ENSP00000483343.1:n.*632-321G>T
|
|
ENST00000619289.4:c.1348G>T
|
ENSP00000484600.1:p.Asp450Tyr
|
|
NM_001282447.1:c.1708G>T
|
NP_001269376.1:p.Asp570Tyr
|
|
NM_025220.3:c.1708G>T
|
NP_079496.1:p.Asp570Tyr
|
|
NM_153202.2:c.1708G>T
|
NP_694882.1:p.Asp570Tyr
|
|
XM_005260843.1:c.1747G>T
|
XP_005260900.1:p.Asp583Tyr
|
|
XM_006723639.1:c.1747G>T
|
XP_006723702.1:p.Asp583Tyr
|
|
XM_006723640.1:c.1738G>T
|
XP_006723703.1:p.Asp580Tyr
|
|
XM_011529366.1:c.1744G>T
|
XP_011527668.1:p.Asp582Tyr
|
|
XM_011529367.1:c.1705G>T
|
XP_011527669.1:p.Asp569Tyr
|
|
XM_011529368.1:c.1747G>T
|
XP_011527670.1:p.Asp583Tyr
|
|
XM_011529369.1:c.1715G>T
|
XP_011527671.1:p.Gly572Val
|
|
XM_011529370.1:c.1715G>T
|
XP_011527672.1:p.Gly572Val
|
|
XM_011529373.1:c.745G>T
|
XP_011527675.1:p.Asp249Tyr
|
|
XR_937151.1:n.1851G>T
|
|
|
XR_937152.1:n.1851G>T
|
|
|
XR_937153.1:n.1732G>T
|
|
|
XR_937154.1:n.1732G>T
|
|
|
XR_937155.1:n.1653G>T
|
|
|
XR_937157.1:n.1655G>T
|
|
|
NM_001282447.2:c.1708G>T
|
NP_001269376.1:p.Asp570Tyr
|
|
NM_025220.4:c.1708G>T
|
NP_079496.1:p.Asp570Tyr
|
|
NM_153202.3:c.1708G>T
|
NP_694882.1:p.Asp570Tyr
|
|
XM_011529373.2:c.745G>T
|
XP_011527675.1:p.Asp249Tyr
|
|
XR_001754405.1:n.1819G>T
|
|
|
XR_002958534.1:n.1928G>T
|
|
|
NM_001282447.3:c.1708G>T
|
NP_001269376.1:p.Asp570Tyr
|
|
NM_025220.5:c.1708G>T
MANE Select
|
NP_079496.1:p.Asp570Tyr
|
|
NM_153202.4:c.1708G>T
|
NP_694882.1:p.Asp570Tyr
|
|