|
ENST00000567027.6:c.*116A>G
|
ENSP00000457521.2:n.*116A>G
|
|
|
ENST00000682061.1:c.*1802A>G
|
ENSP00000508316.1:n.*1802A>G
|
|
|
ENST00000682064.1:n.1683A>G
|
|
|
|
ENST00000682177.1:c.1499A>G
|
ENSP00000507409.1:n.1499A>G
|
|
|
ENST00000682235.1:n.1479A>G
|
|
|
|
ENST00000682461.1:c.1562A>G
|
ENSP00000507308.1:n.1562A>G
|
|
|
ENST00000682653.1:n.2460A>G
|
|
|
|
ENST00000682657.1:c.*1293A>G
|
ENSP00000507753.1:n.*1293A>G
|
|
|
ENST00000682721.1:c.*1259A>G
|
ENSP00000507535.1:n.*1259A>G
|
|
|
ENST00000682843.1:c.*1097A>G
|
ENSP00000508173.1:n.*1097A>G
|
|
|
ENST00000683003.1:c.*1293A>G
|
ENSP00000507576.1:n.*1293A>G
|
|
|
ENST00000683133.1:c.1640A>G
|
ENSP00000508108.1:n.1640A>G
|
|
|
ENST00000683243.1:c.*609A>G
|
ENSP00000507042.1:n.*609A>G
|
|
|
ENST00000683463.1:c.*945A>G
|
ENSP00000507986.1:n.*945A>G
|
|
|
ENST00000683548.1:n.1914A>G
|
|
|
|
ENST00000683579.1:c.*1354A>G
|
ENSP00000506867.1:n.*1354A>G
|
|
|
ENST00000683587.1:n.1987A>G
|
|
|
|
ENST00000683681.1:c.*134A>G
|
ENSP00000508110.1:n.*134A>G
|
|
|
ENST00000683735.1:c.*1854A>G
|
ENSP00000508336.1:n.*1854A>G
|
|
|
ENST00000683853.1:c.*261A>G
|
ENSP00000506834.1:n.*261A>G
|
|
|
ENST00000683860.1:c.*576A>G
|
ENSP00000507179.1:n.*576A>G
|
|
|
ENST00000683884.1:c.*783A>G
|
ENSP00000507004.1:n.*783A>G
|
|
|
ENST00000684041.1:c.*589A>G
|
ENSP00000508382.1:n.*589A>G
|
|
|
ENST00000684125.1:c.*116A>G
|
ENSP00000507320.1:n.*116A>G
|
|
|
ENST00000684203.1:n.3905A>G
|
|
|
|
ENST00000684231.1:c.*866A>G
|
ENSP00000507748.1:n.*866A>G
|
|
|
ENST00000684263.1:c.*1080A>G
|
ENSP00000508369.1:n.*1080A>G
|
|
|
ENST00000684305.1:c.1904A>G
|
ENSP00000506819.1:n.1904A>G
|
|
|
ENST00000684415.1:c.*1007A>G
|
ENSP00000507227.1:n.*1007A>G
|
|
|
ENST00000684520.1:c.*715A>G
|
ENSP00000506826.1:n.*715A>G
|
|
|
ENST00000684602.1:c.*1122A>G
|
ENSP00000507996.1:n.*1122A>G
|
|
|
ENST00000684667.1:c.1787A>G
|
ENSP00000507003.1:n.1787A>G
|
|
|
ENST00000268097.10:c.1456A>G
MANE Select
|
ENSP00000268097.6:p.Ser486Gly
|
|
|
ENST00000268097.9:c.1456A>G
|
ENSP00000268097.5:p.Ser486Gly
|
|
|
ENST00000379915.4:c.538A>G
|
ENSP00000478716.1:p.Ser180Gly
|
|
|
ENST00000564677.5:n.248A>G
|
|
|
|
ENST00000565873.1:n.367A>G
|
|
|
|
ENST00000566304.5:c.1489A>G
|
ENSP00000455114.1:p.Ser497Gly
|
|
|
ENST00000567027.5:c.1071A>G
|
|
|
|
ENST00000567159.5:c.1456A>G
|
ENSP00000456489.1:p.Ser486Gly
|
|
|
ENST00000567411.5:c.*977A>G
|
ENSP00000455545.1:n.*977A>G
|
|
|
ENST00000568777.5:n.6676A>G
|
|
|
|
ENST00000569116.1:n.163A>G
|
|
|
|
NM_000520.4:c.1456A>G
|
NP_000511.2:p.Ser486Gly
|
|
|
NM_000520.5:c.1456A>G
|
NP_000511.2:p.Ser486Gly
|
|
|
NM_001318825.1:c.1489A>G
|
NP_001305754.1:p.Ser497Gly
|
|
|
NR_134869.1:n.1700A>G
|
|
|
|
NM_000520.6:c.1456A>G
MANE Select
|
NP_000511.2:p.Ser486Gly
|
|
|
NM_001318825.2:c.1489A>G
|
NP_001305754.1:p.Ser497Gly
|
|
|
NR_134869.2:n.1241A>G
|
|
|
|
NR_134869.3:n.1241A>G
|
|
|
