|
ENST00000567027.6:c.1074-207T>G
|
ENSP00000457521.2:n.1074-207T>G
|
|
|
ENST00000682061.1:c.*987T>G
|
ENSP00000508316.1:n.*987T>G
|
|
|
ENST00000682064.1:n.667T>G
|
|
|
|
ENST00000682177.1:c.1368T>G
|
ENSP00000507409.1:n.1368T>G
|
|
|
ENST00000682235.1:n.664T>G
|
|
|
|
ENST00000682461.1:c.1431T>G
|
ENSP00000507308.1:n.1431T>G
|
|
|
ENST00000682653.1:n.1645T>G
|
|
|
|
ENST00000682657.1:c.*484-207T>G
|
ENSP00000507753.1:n.*484-207T>G
|
|
|
ENST00000682721.1:c.*1128T>G
|
ENSP00000507535.1:n.*1128T>G
|
|
|
ENST00000682843.1:c.*972-207T>G
|
ENSP00000508173.1:n.*972-207T>G
|
|
|
ENST00000683003.1:c.*484-207T>G
|
ENSP00000507576.1:n.*484-207T>G
|
|
|
ENST00000683133.1:c.1509T>G
|
ENSP00000508108.1:n.1509T>G
|
|
|
ENST00000683243.1:c.*484-207T>G
|
ENSP00000507042.1:n.*484-207T>G
|
|
|
ENST00000683463.1:c.*130T>G
|
ENSP00000507986.1:n.*130T>G
|
|
|
ENST00000683548.1:n.1105-207T>G
|
|
|
|
ENST00000683579.1:c.*1223T>G
|
ENSP00000506867.1:n.*1223T>G
|
|
|
ENST00000683587.1:n.1178-207T>G
|
|
|
|
ENST00000683681.1:c.1325T>G
|
ENSP00000508110.1:p.Phe442Cys
|
|
|
ENST00000683735.1:c.*1045-207T>G
|
ENSP00000508336.1:n.*1045-207T>G
|
|
|
ENST00000683853.1:c.*130T>G
|
ENSP00000506834.1:n.*130T>G
|
|
|
ENST00000683860.1:c.1325T>G
|
ENSP00000507179.1:p.Phe442Cys
|
|
|
ENST00000683884.1:c.1147-207T>G
|
ENSP00000507004.1:n.1147-207T>G
|
|
|
ENST00000684041.1:c.1325T>G
|
ENSP00000508382.1:p.Phe442Cys
|
|
|
ENST00000684125.1:c.1074-207T>G
|
ENSP00000507320.1:n.1074-207T>G
|
|
|
ENST00000684203.1:n.3090T>G
|
|
|
|
ENST00000684231.1:c.*735T>G
|
ENSP00000507748.1:n.*735T>G
|
|
|
ENST00000684263.1:c.*265T>G
|
ENSP00000508369.1:n.*265T>G
|
|
|
ENST00000684305.1:c.1773T>G
|
ENSP00000506819.1:n.1773T>G
|
|
|
ENST00000684415.1:c.*192T>G
|
ENSP00000507227.1:n.*192T>G
|
|
|
ENST00000684520.1:c.1325T>G
|
ENSP00000506826.1:p.Phe442Cys
|
|
|
ENST00000684602.1:c.*991T>G
|
ENSP00000507996.1:n.*991T>G
|
|
|
ENST00000684667.1:c.1656T>G
|
ENSP00000507003.1:n.1656T>G
|
|
|
ENST00000268097.10:c.1325T>G
MANE Select
|
ENSP00000268097.6:p.Phe442Cys
|
|
|
ENST00000268097.9:c.1325T>G
|
ENSP00000268097.5:p.Phe442Cys
|
|
|
ENST00000379915.4:c.413-207T>G
|
ENSP00000478716.1:n.413-207T>G
|
|
|
ENST00000563762.5:c.826-207T>G
|
ENSP00000456346.1:n.826-207T>G
|
|
|
ENST00000566304.5:c.1358T>G
|
ENSP00000455114.1:p.Phe453Cys
|
|
|
ENST00000566672.5:c.*735T>G
|
ENSP00000457037.1:n.*735T>G
|
|
|
ENST00000567027.5:c.946-207T>G
|
|
|
|
ENST00000567159.5:c.1325T>G
|
ENSP00000456489.1:p.Phe442Cys
|
|
|
ENST00000567411.5:c.*846T>G
|
ENSP00000455545.1:n.*846T>G
|
|
|
ENST00000568777.5:n.6551-207T>G
|
|
|
|
ENST00000569410.5:c.*130T>G
|
ENSP00000457125.1:n.*130T>G
|
|
|
NM_000520.4:c.1325T>G
|
NP_000511.2:p.Phe442Cys
|
|
|
NM_000520.5:c.1325T>G
|
NP_000511.2:p.Phe442Cys
|
|
|
NM_001318825.1:c.1358T>G
|
NP_001305754.1:p.Phe453Cys
|
|
|
NR_134869.1:n.1575-207T>G
|
|
|
|
NM_000520.6:c.1325T>G
MANE Select
|
NP_000511.2:p.Phe442Cys
|
|
|
NM_001318825.2:c.1358T>G
|
NP_001305754.1:p.Phe453Cys
|
|
|
NR_134869.2:n.1116-207T>G
|
|
|
|
NR_134869.3:n.1116-207T>G
|
|
|
