|
ENST00000567027.6:c.1074-253T>G
|
ENSP00000457521.2:n.1074-253T>G
|
|
|
ENST00000682061.1:c.*941T>G
|
ENSP00000508316.1:n.*941T>G
|
|
|
ENST00000682064.1:n.621T>G
|
|
|
|
ENST00000682177.1:c.1322T>G
|
ENSP00000507409.1:n.1322T>G
|
|
|
ENST00000682235.1:n.618T>G
|
|
|
|
ENST00000682461.1:c.1385T>G
|
ENSP00000507308.1:n.1385T>G
|
|
|
ENST00000682653.1:n.1599T>G
|
|
|
|
ENST00000682657.1:c.*484-253T>G
|
ENSP00000507753.1:n.*484-253T>G
|
|
|
ENST00000682721.1:c.*1082T>G
|
ENSP00000507535.1:n.*1082T>G
|
|
|
ENST00000682843.1:c.*972-253T>G
|
ENSP00000508173.1:n.*972-253T>G
|
|
|
ENST00000683003.1:c.*484-253T>G
|
ENSP00000507576.1:n.*484-253T>G
|
|
|
ENST00000683133.1:c.1463T>G
|
ENSP00000508108.1:n.1463T>G
|
|
|
ENST00000683243.1:c.*484-253T>G
|
ENSP00000507042.1:n.*484-253T>G
|
|
|
ENST00000683463.1:c.*84T>G
|
ENSP00000507986.1:n.*84T>G
|
|
|
ENST00000683548.1:n.1105-253T>G
|
|
|
|
ENST00000683579.1:c.*1177T>G
|
ENSP00000506867.1:n.*1177T>G
|
|
|
ENST00000683587.1:n.1178-253T>G
|
|
|
|
ENST00000683681.1:c.1279T>G
|
ENSP00000508110.1:p.Tyr427Asp
|
|
|
ENST00000683735.1:c.*1045-253T>G
|
ENSP00000508336.1:n.*1045-253T>G
|
|
|
ENST00000683853.1:c.*84T>G
|
ENSP00000506834.1:n.*84T>G
|
|
|
ENST00000683860.1:c.1279T>G
|
ENSP00000507179.1:p.Tyr427Asp
|
|
|
ENST00000683884.1:c.1147-253T>G
|
ENSP00000507004.1:n.1147-253T>G
|
|
|
ENST00000684041.1:c.1279T>G
|
ENSP00000508382.1:p.Tyr427Asp
|
|
|
ENST00000684125.1:c.1074-253T>G
|
ENSP00000507320.1:n.1074-253T>G
|
|
|
ENST00000684203.1:n.3044T>G
|
|
|
|
ENST00000684231.1:c.*689T>G
|
ENSP00000507748.1:n.*689T>G
|
|
|
ENST00000684263.1:c.*219T>G
|
ENSP00000508369.1:n.*219T>G
|
|
|
ENST00000684305.1:c.1727T>G
|
ENSP00000506819.1:n.1727T>G
|
|
|
ENST00000684415.1:c.*146T>G
|
ENSP00000507227.1:n.*146T>G
|
|
|
ENST00000684520.1:c.1279T>G
|
ENSP00000506826.1:p.Tyr427Asp
|
|
|
ENST00000684602.1:c.*945T>G
|
ENSP00000507996.1:n.*945T>G
|
|
|
ENST00000684667.1:c.1610T>G
|
ENSP00000507003.1:n.1610T>G
|
|
|
ENST00000268097.10:c.1279T>G
MANE Select
|
ENSP00000268097.6:p.Tyr427Asp
|
|
|
ENST00000268097.9:c.1279T>G
|
ENSP00000268097.5:p.Tyr427Asp
|
|
|
ENST00000379915.4:c.413-253T>G
|
ENSP00000478716.1:n.413-253T>G
|
|
|
ENST00000563762.5:c.826-253T>G
|
ENSP00000456346.1:n.826-253T>G
|
|
|
ENST00000566304.5:c.1312T>G
|
ENSP00000455114.1:p.Tyr438Asp
|
|
|
ENST00000566672.5:c.*689T>G
|
ENSP00000457037.1:n.*689T>G
|
|
|
ENST00000567027.5:c.946-253T>G
|
|
|
|
ENST00000567159.5:c.1279T>G
|
ENSP00000456489.1:p.Tyr427Asp
|
|
|
ENST00000567411.5:c.*800T>G
|
ENSP00000455545.1:n.*800T>G
|
|
|
ENST00000568777.5:n.6551-253T>G
|
|
|
|
ENST00000569410.5:c.*84T>G
|
ENSP00000457125.1:n.*84T>G
|
|
|
NM_000520.4:c.1279T>G
|
NP_000511.2:p.Tyr427Asp
|
|
|
NM_000520.5:c.1279T>G
|
NP_000511.2:p.Tyr427Asp
|
|
|
NM_001318825.1:c.1312T>G
|
NP_001305754.1:p.Tyr438Asp
|
|
|
NR_134869.1:n.1575-253T>G
|
|
|
|
NM_000520.6:c.1279T>G
MANE Select
|
NP_000511.2:p.Tyr427Asp
|
|
|
NM_001318825.2:c.1312T>G
|
NP_001305754.1:p.Tyr438Asp
|
|
|
NR_134869.2:n.1116-253T>G
|
|
|
|
NR_134869.3:n.1116-253T>G
|
|
|
