|
ENST00000567027.6:c.1074-373A>G
|
ENSP00000457521.2:n.1074-373A>G
|
|
|
ENST00000682061.1:c.*821A>G
|
ENSP00000508316.1:n.*821A>G
|
|
|
ENST00000682064.1:n.501A>G
|
|
|
|
ENST00000682177.1:c.1202A>G
|
ENSP00000507409.1:n.1202A>G
|
|
|
ENST00000682235.1:n.498A>G
|
|
|
|
ENST00000682461.1:c.1265A>G
|
ENSP00000507308.1:n.1265A>G
|
|
|
ENST00000682653.1:n.1479A>G
|
|
|
|
ENST00000682657.1:c.*484-373A>G
|
ENSP00000507753.1:n.*484-373A>G
|
|
|
ENST00000682721.1:c.*962A>G
|
ENSP00000507535.1:n.*962A>G
|
|
|
ENST00000682843.1:c.*972-373A>G
|
ENSP00000508173.1:n.*972-373A>G
|
|
|
ENST00000683003.1:c.*484-373A>G
|
ENSP00000507576.1:n.*484-373A>G
|
|
|
ENST00000683133.1:c.1343A>G
|
ENSP00000508108.1:n.1343A>G
|
|
|
ENST00000683243.1:c.*484-373A>G
|
ENSP00000507042.1:n.*484-373A>G
|
|
|
ENST00000683463.1:c.1086A>G
|
ENSP00000507986.1:p.Thr362=
|
|
|
ENST00000683548.1:n.1105-373A>G
|
|
|
|
ENST00000683579.1:c.*1057A>G
|
ENSP00000506867.1:n.*1057A>G
|
|
|
ENST00000683587.1:n.1178-373A>G
|
|
|
|
ENST00000683681.1:c.1159A>G
|
ENSP00000508110.1:p.Thr387Ala
|
|
|
ENST00000683735.1:c.*1045-373A>G
|
ENSP00000508336.1:n.*1045-373A>G
|
|
|
ENST00000683853.1:c.1086A>G
|
ENSP00000506834.1:p.Thr362=
|
|
|
ENST00000683860.1:c.1159A>G
|
ENSP00000507179.1:p.Thr387Ala
|
|
|
ENST00000683884.1:c.1147-373A>G
|
ENSP00000507004.1:n.1147-373A>G
|
|
|
ENST00000684041.1:c.1159A>G
|
ENSP00000508382.1:p.Thr387Ala
|
|
|
ENST00000684125.1:c.1074-373A>G
|
ENSP00000507320.1:n.1074-373A>G
|
|
|
ENST00000684203.1:n.2924A>G
|
|
|
|
ENST00000684231.1:c.*569A>G
|
ENSP00000507748.1:n.*569A>G
|
|
|
ENST00000684263.1:c.*99A>G
|
ENSP00000508369.1:n.*99A>G
|
|
|
ENST00000684305.1:c.1607A>G
|
ENSP00000506819.1:n.1607A>G
|
|
|
ENST00000684415.1:c.*26A>G
|
ENSP00000507227.1:n.*26A>G
|
|
|
ENST00000684520.1:c.1159A>G
|
ENSP00000506826.1:p.Thr387Ala
|
|
|
ENST00000684602.1:c.*825A>G
|
ENSP00000507996.1:n.*825A>G
|
|
|
ENST00000684667.1:c.1490A>G
|
ENSP00000507003.1:n.1490A>G
|
|
|
ENST00000268097.10:c.1159A>G
MANE Select
|
ENSP00000268097.6:p.Thr387Ala
|
|
|
ENST00000268097.9:c.1159A>G
|
ENSP00000268097.5:p.Thr387Ala
|
|
|
ENST00000379915.4:c.413-373A>G
|
ENSP00000478716.1:n.413-373A>G
|
|
|
ENST00000563762.5:c.826-373A>G
|
ENSP00000456346.1:n.826-373A>G
|
|
|
ENST00000566304.5:c.1192A>G
|
ENSP00000455114.1:p.Thr398Ala
|
|
|
ENST00000566672.5:c.*569A>G
|
ENSP00000457037.1:n.*569A>G
|
|
|
ENST00000567027.5:c.946-373A>G
|
|
|
|
ENST00000567159.5:c.1159A>G
|
ENSP00000456489.1:p.Thr387Ala
|
|
|
ENST00000567411.5:c.*680A>G
|
ENSP00000455545.1:n.*680A>G
|
|
|
ENST00000568777.5:n.6551-373A>G
|
|
|
|
ENST00000569410.5:c.1086A>G
|
ENSP00000457125.1:p.Thr362=
|
|
|
NM_000520.4:c.1159A>G
|
NP_000511.2:p.Thr387Ala
|
|
|
NM_000520.5:c.1159A>G
|
NP_000511.2:p.Thr387Ala
|
|
|
NM_001318825.1:c.1192A>G
|
NP_001305754.1:p.Thr398Ala
|
|
|
NR_134869.1:n.1575-373A>G
|
|
|
|
NM_000520.6:c.1159A>G
MANE Select
|
NP_000511.2:p.Thr387Ala
|
|
|
NM_001318825.2:c.1192A>G
|
NP_001305754.1:p.Thr398Ala
|
|
|
NR_134869.2:n.1116-373A>G
|
|
|
|
NR_134869.3:n.1116-373A>G
|
|
|
