ENST00000567027.6:c.*82-223G>T
|
ENSP00000457521.2:n.*82-223G>T
|
|
ENST00000682061.1:c.*1545G>T
|
ENSP00000508316.1:n.*1545G>T
|
|
ENST00000682064.1:n.1426G>T
|
|
|
ENST00000682177.1:c.1465-223G>T
|
ENSP00000507409.1:n.1465-223G>T
|
|
ENST00000682235.1:n.1222G>T
|
|
|
ENST00000682461.1:c.1528-223G>T
|
ENSP00000507308.1:n.1528-223G>T
|
|
ENST00000682653.1:n.2203G>T
|
|
|
ENST00000682657.1:c.*1036G>T
|
ENSP00000507753.1:n.*1036G>T
|
|
ENST00000682721.1:c.*1225-223G>T
|
ENSP00000507535.1:n.*1225-223G>T
|
|
ENST00000682843.1:c.*1063-223G>T
|
ENSP00000508173.1:n.*1063-223G>T
|
|
ENST00000683003.1:c.*1036G>T
|
ENSP00000507576.1:n.*1036G>T
|
|
ENST00000683133.1:c.1606-223G>T
|
ENSP00000508108.1:n.1606-223G>T
|
|
ENST00000683243.1:c.*575-223G>T
|
ENSP00000507042.1:n.*575-223G>T
|
|
ENST00000683463.1:c.*688G>T
|
ENSP00000507986.1:n.*688G>T
|
|
ENST00000683548.1:n.1657G>T
|
|
|
ENST00000683579.1:c.*1320-223G>T
|
ENSP00000506867.1:n.*1320-223G>T
|
|
ENST00000683587.1:n.1730G>T
|
|
|
ENST00000683681.1:c.*3G>T
|
ENSP00000508110.1:n.*3G>T
|
|
ENST00000683735.1:c.*1597G>T
|
ENSP00000508336.1:n.*1597G>T
|
|
ENST00000683853.1:c.*227-223G>T
|
ENSP00000506834.1:n.*227-223G>T
|
|
ENST00000683860.1:c.*319G>T
|
ENSP00000507179.1:n.*319G>T
|
|
ENST00000683884.1:c.*526G>T
|
ENSP00000507004.1:n.*526G>T
|
|
ENST00000684041.1:c.*458G>T
|
ENSP00000508382.1:n.*458G>T
|
|
ENST00000684125.1:c.*82-223G>T
|
ENSP00000507320.1:n.*82-223G>T
|
|
ENST00000684203.1:n.3648G>T
|
|
|
ENST00000684231.1:c.*832-223G>T
|
ENSP00000507748.1:n.*832-223G>T
|
|
ENST00000684263.1:c.*823G>T
|
ENSP00000508369.1:n.*823G>T
|
|
ENST00000684305.1:c.1870-223G>T
|
ENSP00000506819.1:n.1870-223G>T
|
|
ENST00000684415.1:c.*750G>T
|
ENSP00000507227.1:n.*750G>T
|
|
ENST00000684520.1:c.*458G>T
|
ENSP00000506826.1:n.*458G>T
|
|
ENST00000684602.1:c.*1088-223G>T
|
ENSP00000507996.1:n.*1088-223G>T
|
|
ENST00000684667.1:c.1753-223G>T
|
ENSP00000507003.1:n.1753-223G>T
|
|
ENST00000268097.10:c.1422-223G>T
MANE Select
|
ENSP00000268097.6:n.1422-223G>T
|
|
ENST00000268097.9:c.1422-223G>T
|
ENSP00000268097.5:n.1422-223G>T
|
|
ENST00000379915.4:c.504-223G>T
|
ENSP00000478716.1:n.504-223G>T
|
|
ENST00000564677.5:n.117G>T
|
|
|
ENST00000565873.1:n.110G>T
|
|
|
ENST00000566304.5:c.1455-223G>T
|
ENSP00000455114.1:n.1455-223G>T
|
|
ENST00000567027.5:c.1037-223G>T
|
|
|
ENST00000567159.5:c.1422-223G>T
|
ENSP00000456489.1:n.1422-223G>T
|
|
ENST00000567411.5:c.*943-223G>T
|
ENSP00000455545.1:n.*943-223G>T
|
|
ENST00000568777.5:n.6642-223G>T
|
|
|
ENST00000569116.1:n.32G>T
|
|
|
NM_000520.4:c.1422-223G>T
|
NP_000511.2:n.1422-223G>T
|
|
NM_000520.5:c.1422-223G>T
|
NP_000511.2:n.1422-223G>T
|
|
NM_001318825.1:c.1455-223G>T
|
NP_001305754.1:n.1455-223G>T
|
|
NR_134869.1:n.1666-223G>T
|
|
|
NM_000520.6:c.1422-223G>T
MANE Select
|
NP_000511.2:n.1422-223G>T
|
|
NM_001318825.2:c.1455-223G>T
|
NP_001305754.1:n.1455-223G>T
|
|
NR_134869.2:n.1207-223G>T
|
|
|
NR_134869.3:n.1207-223G>T
|
|
|