|
ENST00000567027.6:c.*161T>G
|
ENSP00000457521.2:n.*161T>G
|
|
|
ENST00000682061.1:c.*1847T>G
|
ENSP00000508316.1:n.*1847T>G
|
|
|
ENST00000682064.1:n.1728T>G
|
|
|
|
ENST00000682177.1:c.1544T>G
|
ENSP00000507409.1:n.1544T>G
|
|
|
ENST00000682235.1:n.1524T>G
|
|
|
|
ENST00000682461.1:c.1607T>G
|
ENSP00000507308.1:n.1607T>G
|
|
|
ENST00000682653.1:n.2505T>G
|
|
|
|
ENST00000682657.1:c.*1338T>G
|
ENSP00000507753.1:n.*1338T>G
|
|
|
ENST00000682721.1:c.*1304T>G
|
ENSP00000507535.1:n.*1304T>G
|
|
|
ENST00000682843.1:c.*1142T>G
|
ENSP00000508173.1:n.*1142T>G
|
|
|
ENST00000683003.1:c.*1338T>G
|
ENSP00000507576.1:n.*1338T>G
|
|
|
ENST00000683133.1:c.1685T>G
|
ENSP00000508108.1:n.1685T>G
|
|
|
ENST00000683243.1:c.*654T>G
|
ENSP00000507042.1:n.*654T>G
|
|
|
ENST00000683463.1:c.*990T>G
|
ENSP00000507986.1:n.*990T>G
|
|
|
ENST00000683548.1:n.1959T>G
|
|
|
|
ENST00000683579.1:c.*1399T>G
|
ENSP00000506867.1:n.*1399T>G
|
|
|
ENST00000683587.1:n.2032T>G
|
|
|
|
ENST00000683681.1:c.*179T>G
|
ENSP00000508110.1:n.*179T>G
|
|
|
ENST00000683735.1:c.*1899T>G
|
ENSP00000508336.1:n.*1899T>G
|
|
|
ENST00000683853.1:c.*306T>G
|
ENSP00000506834.1:n.*306T>G
|
|
|
ENST00000683860.1:c.*621T>G
|
ENSP00000507179.1:n.*621T>G
|
|
|
ENST00000683884.1:c.*828T>G
|
ENSP00000507004.1:n.*828T>G
|
|
|
ENST00000684041.1:c.*634T>G
|
ENSP00000508382.1:n.*634T>G
|
|
|
ENST00000684125.1:c.*161T>G
|
ENSP00000507320.1:n.*161T>G
|
|
|
ENST00000684203.1:n.3950T>G
|
|
|
|
ENST00000684231.1:c.*911T>G
|
ENSP00000507748.1:n.*911T>G
|
|
|
ENST00000684263.1:c.*1125T>G
|
ENSP00000508369.1:n.*1125T>G
|
|
|
ENST00000684305.1:c.1949T>G
|
ENSP00000506819.1:n.1949T>G
|
|
|
ENST00000684415.1:c.*1052T>G
|
ENSP00000507227.1:n.*1052T>G
|
|
|
ENST00000684520.1:c.*760T>G
|
ENSP00000506826.1:n.*760T>G
|
|
|
ENST00000684602.1:c.*1167T>G
|
ENSP00000507996.1:n.*1167T>G
|
|
|
ENST00000684667.1:c.1832T>G
|
ENSP00000507003.1:n.1832T>G
|
|
|
ENST00000268097.10:c.1501T>G
MANE Select
|
ENSP00000268097.6:p.Ser501Ala
|
|
|
ENST00000268097.9:c.1501T>G
|
ENSP00000268097.5:p.Ser501Ala
|
|
|
ENST00000379915.4:c.583T>G
|
ENSP00000478716.1:p.Ser195Ala
|
|
|
ENST00000564677.5:n.293T>G
|
|
|
|
ENST00000565873.1:n.412T>G
|
|
|
|
ENST00000566304.5:c.1534T>G
|
ENSP00000455114.1:p.Ser512Ala
|
|
|
ENST00000567027.5:c.1116T>G
|
|
|
|
ENST00000567159.5:c.1501T>G
|
ENSP00000456489.1:p.Ser501Ala
|
|
|
ENST00000567411.5:c.*1022T>G
|
ENSP00000455545.1:n.*1022T>G
|
|
|
ENST00000568777.5:n.6721T>G
|
|
|
|
ENST00000569116.1:n.208T>G
|
|
|
|
NM_000520.4:c.1501T>G
|
NP_000511.2:p.Ser501Ala
|
|
|
NM_000520.5:c.1501T>G
|
NP_000511.2:p.Ser501Ala
|
|
|
NM_001318825.1:c.1534T>G
|
NP_001305754.1:p.Ser512Ala
|
|
|
NR_134869.1:n.1745T>G
|
|
|
|
NM_000520.6:c.1501T>G
MANE Select
|
NP_000511.2:p.Ser501Ala
|
|
|
NM_001318825.2:c.1534T>G
|
NP_001305754.1:p.Ser512Ala
|
|
|
NR_134869.2:n.1286T>G
|
|
|
|
NR_134869.3:n.1286T>G
|
|
|
