|
ENST00000563908.2:n.2967T=
|
|
|
|
ENST00000567027.6:c.621T=
|
ENSP00000457521.2:p.Asp207=
|
|
|
ENST00000568260.2:c.641T=
|
ENSP00000458128.2:n.641T=
|
|
|
ENST00000682061.1:c.*283T=
|
ENSP00000508316.1:n.*283T=
|
|
|
ENST00000682177.1:c.621T=
|
ENSP00000507409.1:p.Asp207=
|
|
|
ENST00000682461.1:c.727T=
|
ENSP00000507308.1:n.727T=
|
|
|
ENST00000682653.1:n.652T=
|
|
|
|
ENST00000682657.1:c.*31T=
|
ENSP00000507753.1:n.*31T=
|
|
|
ENST00000682721.1:c.*424T=
|
ENSP00000507535.1:n.*424T=
|
|
|
ENST00000682843.1:c.*519T=
|
ENSP00000508173.1:n.*519T=
|
|
|
ENST00000683003.1:c.*31T=
|
ENSP00000507576.1:n.*31T=
|
|
|
ENST00000683133.1:c.805T=
|
ENSP00000508108.1:n.805T=
|
|
|
ENST00000683228.1:n.652T=
|
|
|
|
ENST00000683243.1:c.*31T=
|
ENSP00000507042.1:n.*31T=
|
|
|
ENST00000683463.1:c.621T=
|
ENSP00000507986.1:p.Asp207=
|
|
|
ENST00000683548.1:n.652T=
|
|
|
|
ENST00000683579.1:c.*519T=
|
ENSP00000506867.1:n.*519T=
|
|
|
ENST00000683587.1:n.652T=
|
|
|
|
ENST00000683681.1:c.621T=
|
ENSP00000508110.1:p.Asp207=
|
|
|
ENST00000683735.1:c.*519T=
|
ENSP00000508336.1:n.*519T=
|
|
|
ENST00000683742.1:n.452T=
|
|
|
|
ENST00000683853.1:c.621T=
|
ENSP00000506834.1:p.Asp207=
|
|
|
ENST00000683860.1:c.621T=
|
ENSP00000507179.1:p.Asp207=
|
|
|
ENST00000683884.1:c.621T=
|
ENSP00000507004.1:p.Asp207=
|
|
|
ENST00000684041.1:c.621T=
|
ENSP00000508382.1:p.Asp207=
|
|
|
ENST00000684125.1:c.621T=
|
ENSP00000507320.1:p.Asp207=
|
|
|
ENST00000684203.1:n.2459T=
|
|
|
|
ENST00000684231.1:c.*31T=
|
ENSP00000507748.1:n.*31T=
|
|
|
ENST00000684263.1:c.621T=
|
ENSP00000508369.1:p.Asp207=
|
|
|
ENST00000684305.1:c.1069T=
|
ENSP00000506819.1:n.1069T=
|
|
|
ENST00000684415.1:c.621T=
|
ENSP00000507227.1:p.Asp207=
|
|
|
ENST00000684520.1:c.621T=
|
ENSP00000506826.1:p.Asp207=
|
|
|
ENST00000684602.1:c.*287T=
|
ENSP00000507996.1:n.*287T=
|
|
|
ENST00000684667.1:c.952T=
|
ENSP00000507003.1:n.952T=
|
|
|
ENST00000268097.10:c.621T=
MANE Select
|
ENSP00000268097.6:p.Asp207=
|
|
|
ENST00000268097.9:c.621T=
|
ENSP00000268097.5:p.Asp207=
|
|
|
ENST00000379915.4:c.412+4375T=
|
ENSP00000478716.1:n.412+4375T=
|
|
|
ENST00000563762.5:c.554T=
|
ENSP00000456346.1:n.554T=
|
|
|
ENST00000566304.5:c.654T=
|
ENSP00000455114.1:p.Asp218=
|
|
|
ENST00000566672.5:c.*31T=
|
ENSP00000457037.1:n.*31T=
|
|
|
ENST00000567027.5:c.493T=
|
|
|
|
ENST00000567159.5:c.621T=
|
ENSP00000456489.1:p.Asp207=
|
|
|
ENST00000567411.5:c.*142T=
|
ENSP00000455545.1:n.*142T=
|
|
|
ENST00000568260.1:c.622T=
|
|
|
|
ENST00000568777.5:n.6025T=
|
|
|
|
ENST00000569410.5:c.621T=
|
ENSP00000457125.1:p.Asp207=
|
|
|
ENST00000569509.5:n.468T=
|
|
|
|
NM_000520.4:c.621T=
|
NP_000511.2:p.Asp207=
|
|
|
NM_000520.5:c.621T=
|
NP_000511.2:p.Asp207=
|
|
|
NM_001318825.1:c.654T=
|
NP_001305754.1:p.Asp218=
|
|
|
NR_134869.1:n.1122T=
|
|
|
|
NM_000520.6:c.621T=
MANE Select
|
NP_000511.2:p.Asp207=
|
|
|
NM_001318825.2:c.654T=
|
NP_001305754.1:p.Asp218=
|
|
|
NR_134869.2:n.663T=
|
|
|
|
NR_134869.3:n.663T=
|
|
|
