ENST00000492931.6:n.1193G>A
(ADA)
|
|
|
ENST00000536076.2:c.873G>A
(ADA)
|
ENSP00000512234.1:p.Glu291=
|
|
ENST00000536532.6:c.*169G>A
(ADA)
|
ENSP00000440946.1:n.*169G>A
|
|
ENST00000537820.2:c.954G>A
(ADA)
|
ENSP00000441818.1:p.Glu318=
|
|
ENST00000539235.6:c.*410G>A
(ADA)
|
ENSP00000446464.1:n.*410G>A
|
|
ENST00000695889.1:c.501G>A
(ADA)
|
ENSP00000512240.1:p.Glu167=
|
|
ENST00000695890.1:n.5137G>A
(ADA)
|
|
|
ENST00000695891.1:c.566G>A
(ADA)
|
ENSP00000512241.1:n.566G>A
|
|
ENST00000695927.1:c.1104G>A
(ADA)
|
ENSP00000512270.1:p.Glu368=
|
|
ENST00000695949.1:c.951G>A
(ADA)
|
ENSP00000512281.1:p.Glu317=
|
|
ENST00000695956.1:c.181G>A
(ADA)
|
|
|
ENST00000695957.1:c.*517G>A
(ADA)
|
ENSP00000512286.1:n.*517G>A
|
|
ENST00000695991.1:c.564G>A
(ADA)
|
ENSP00000512314.1:p.Glu188=
|
|
ENST00000695992.1:c.*169G>A
(ADA)
|
ENSP00000512315.1:n.*169G>A
|
|
ENST00000695993.1:c.1026G>A
(ADA)
|
ENSP00000512316.1:p.Glu342=
|
|
ENST00000695994.1:c.*169G>A
(ADA)
|
ENSP00000512317.1:n.*169G>A
|
|
ENST00000695995.1:c.636G>A
(ADA)
|
ENSP00000512318.1:p.Glu212=
|
|
ENST00000695996.1:n.1108G>A
(ADA)
|
|
|
ENST00000696003.1:n.2810G>A
(ADA)
|
|
|
ENST00000696004.1:n.1810G>A
(ADA)
|
|
|
ENST00000696005.1:c.476G>A
(ADA)
|
|
|
ENST00000696006.1:c.*169G>A
(ADA)
|
ENSP00000512325.1:n.*169G>A
|
|
ENST00000696007.1:c.953G>A
(ADA)
|
ENSP00000512326.1:n.953G>A
|
|
ENST00000696008.1:n.3380G>A
(ADA)
|
|
|
ENST00000696017.1:c.1023G>A
(ADA)
|
ENSP00000512333.1:p.Glu341=
|
|
ENST00000696034.1:c.*169G>A
(ADA)
|
ENSP00000512343.1:n.*169G>A
|
|
ENST00000696035.1:n.1212G>A
(ADA)
|
|
|
ENST00000696036.1:n.1727G>A
(ADA)
|
|
|
ENST00000696037.1:n.2703G>A
(ADA)
|
|
|
ENST00000696038.1:c.*783G>A
(ADA)
|
ENSP00000512344.1:n.*783G>A
|
|
ENST00000696039.1:n.1390G>A
(ADA)
|
|
|
ENST00000696058.1:c.1023G>A
(ADA)
|
ENSP00000512361.1:p.Glu341=
|
|
ENST00000696059.1:c.*971G>A
(ADA)
|
ENSP00000512362.1:n.*971G>A
|
|
ENST00000696060.1:c.1095G>A
(ADA)
|
ENSP00000512363.1:p.Glu365=
|
|
ENST00000696061.1:c.1023G>A
(ADA)
|
ENSP00000512364.1:p.Glu341=
|
|
ENST00000696062.1:c.1089G>A
(ADA)
|
ENSP00000512365.1:p.Glu363=
|
|
ENST00000696063.1:c.1101G>A
(ADA)
|
ENSP00000512366.1:p.Glu367=
|
|
ENST00000696064.1:c.873G>A
(ADA)
|
ENSP00000512367.1:p.Glu291=
|
|
ENST00000696065.1:c.348G>A
(ADA)
|
ENSP00000512368.1:p.Glu116=
|
|
ENST00000696072.1:n.381G>A
(ADA)
|
|
|
ENST00000696073.1:n.1337G>A
(ADA)
|
|
|
ENST00000696074.1:n.577G>A
(ADA)
|
|
|
ENST00000696075.1:c.*996G>A
(ADA)
|
ENSP00000512374.1:n.*996G>A
|
|
ENST00000696076.1:c.1095G>A
(ADA)
|
ENSP00000512375.1:p.Glu365=
|
|
ENST00000696077.1:c.1020G>A
(ADA)
|
ENSP00000512376.1:p.Glu340=
|
|
ENST00000696078.1:c.1023G>A
(ADA)
|
ENSP00000512377.1:p.Glu341=
|
|
ENST00000696079.1:c.1023G>A
(ADA)
|
ENSP00000512378.1:p.Glu341=
|
|
ENST00000696080.1:c.1026G>A
(ADA)
|
ENSP00000512379.1:p.Glu342=
|
|
ENST00000696081.1:n.1145G>A
(ADA)
|
|
|
ENST00000696082.1:c.1101G>A
(ADA)
|
ENSP00000512380.1:p.Glu367=
|
|
ENST00000696083.1:n.1983G>A
(ADA)
|
|
|
ENST00000696084.1:n.1203G>A
(ADA)
|
|
|
ENST00000696104.1:c.*95G>A
(ADA)
|
ENSP00000512399.1:n.*95G>A
|
|
ENST00000372874.9:c.1026G>A
(ADA)
MANE Select
|
ENSP00000361965.4:p.Glu342=
|
|
ENST00000372874.8:c.1026G>A
(ADA)
|
ENSP00000361965.4:p.Glu342=
|
|
ENST00000372887.5:c.152-3582C>T
(PKIG)
|
ENSP00000361978.1:n.152-3582C>T
|
|
ENST00000464097.5:n.1392G>A
(ADA)
|
|
|
ENST00000492931.5:n.1186G>A
(ADA)
|
|
|
ENST00000536532.5:c.*169G>A
(ADA)
|
ENSP00000440946.1:n.*169G>A
|
|
ENST00000537820.1:c.954G>A
(ADA)
|
ENSP00000441818.1:p.Glu318=
|
|
ENST00000539235.5:c.*410G>A
(ADA)
|
ENSP00000446464.1:n.*410G>A
|
|
NM_000022.2:c.1026G>A , LRG_16t1:c.1026G>A
(ADA)
|
NP_000013.2:p.Glu342=
|
|
XM_005260236.2:c.954G>A
(ADA)
|
XP_005260293.1:p.Glu318=
|
|
XM_011528478.1:c.621G>A
(ADA)
|
XP_011526780.1:p.Glu207=
|
|
XM_011528479.1:c.621G>A
(ADA)
|
XP_011526781.1:p.Glu207=
|
|
XR_244129.1:n.1015G>A
(ADA)
|
|
|
NM_000022.3:c.1026G>A
(ADA)
|
NP_000013.2:p.Glu342=
|
|
NM_001322050.1:c.621G>A
(ADA)
|
NP_001308979.1:p.Glu207=
|
|
NM_001322051.1:c.954G>A
(ADA)
|
NP_001308980.1:p.Glu318=
|
|
NR_136160.1:n.1112G>A
(ADA)
|
|
|
NM_000022.4:c.1026G>A
(ADA)
MANE Select
|
NP_000013.2:p.Glu342=
|
|
NM_001322050.2:c.621G>A
(ADA)
|
NP_001308979.1:p.Glu207=
|
|
NM_001322051.2:c.954G>A
(ADA)
|
NP_001308980.1:p.Glu318=
|
|
NR_136160.2:n.1053G>A
(ADA)
|
|
|