ENST00000356518.7:c.2325G>T
MANE Select
|
ENSP00000348912.3:p.Trp775Cys
|
|
ENST00000350009.6:c.2247G>T
|
ENSP00000322550.5:p.Trp749Cys
|
|
ENST00000356518.6:c.2325G>T
|
ENSP00000348912.2:p.Trp775Cys
|
|
ENST00000379861.8:c.2325G>T
|
ENSP00000369190.4:p.Trp775Cys
|
|
ENST00000466620.5:n.1886G>T
|
|
|
ENST00000483362.1:n.1073G>T
|
|
|
ENST00000617732.1:c.*1012G>T
|
ENSP00000483343.1:n.*1012G>T
|
|
ENST00000619289.4:c.1965G>T
|
ENSP00000484600.1:p.Trp655Cys
|
|
NM_001282447.1:c.2325G>T
|
NP_001269376.1:p.Trp775Cys
|
|
NM_025220.3:c.2325G>T
|
NP_079496.1:p.Trp775Cys
|
|
NM_153202.2:c.2247G>T
|
NP_694882.1:p.Trp749Cys
|
|
XM_005260843.1:c.2364G>T
|
XP_005260900.1:p.Trp788Cys
|
|
XM_006723639.1:c.2364G>T
|
XP_006723702.1:p.Trp788Cys
|
|
XM_006723640.1:c.2355G>T
|
XP_006723703.1:p.Trp785Cys
|
|
XM_011529366.1:c.2361G>T
|
XP_011527668.1:p.Trp787Cys
|
|
XM_011529367.1:c.2322G>T
|
XP_011527669.1:p.Trp774Cys
|
|
XM_011529368.1:c.2286G>T
|
XP_011527670.1:p.Trp762Cys
|
|
XM_011529373.1:c.1362G>T
|
XP_011527675.1:p.Trp454Cys
|
|
XR_937151.1:n.2384-183G>T
|
|
|
XR_937152.1:n.2384-183G>T
|
|
|
XR_937153.1:n.2349G>T
|
|
|
XR_937154.1:n.2349G>T
|
|
|
XR_937155.1:n.2270G>T
|
|
|
XR_937157.1:n.2272G>T
|
|
|
NM_001282447.2:c.2325G>T
|
NP_001269376.1:p.Trp775Cys
|
|
NM_025220.4:c.2325G>T
|
NP_079496.1:p.Trp775Cys
|
|
NM_153202.3:c.2247G>T
|
NP_694882.1:p.Trp749Cys
|
|
XM_011529373.2:c.1362G>T
|
XP_011527675.1:p.Trp454Cys
|
|
XR_001754405.1:n.2436G>T
|
|
|
XR_002958534.1:n.2545G>T
|
|
|
NM_001282447.3:c.2325G>T
|
NP_001269376.1:p.Trp775Cys
|
|
NM_025220.5:c.2325G>T
MANE Select
|
NP_079496.1:p.Trp775Cys
|
|
NM_153202.4:c.2247G>T
|
NP_694882.1:p.Trp749Cys
|
|