ENST00000492931.6:n.1170C>G
(ADA)
|
|
|
ENST00000536076.2:c.850C>G
(ADA)
|
ENSP00000512234.1:p.Leu284Val
|
|
ENST00000536532.6:c.*146C>G
(ADA)
|
ENSP00000440946.1:n.*146C>G
|
|
ENST00000537820.2:c.931C>G
(ADA)
|
ENSP00000441818.1:p.Leu311Val
|
|
ENST00000539235.6:c.*387C>G
(ADA)
|
ENSP00000446464.1:n.*387C>G
|
|
ENST00000695889.1:c.478C>G
(ADA)
|
ENSP00000512240.1:p.Leu160Val
|
|
ENST00000695890.1:n.5114C>G
(ADA)
|
|
|
ENST00000695891.1:c.543C>G
(ADA)
|
ENSP00000512241.1:n.543C>G
|
|
ENST00000695927.1:c.1081C>G
(ADA)
|
ENSP00000512270.1:p.Leu361Val
|
|
ENST00000695949.1:c.928C>G
(ADA)
|
ENSP00000512281.1:p.Leu310Val
|
|
ENST00000695956.1:c.158C>G
(ADA)
|
|
|
ENST00000695957.1:c.*494C>G
(ADA)
|
ENSP00000512286.1:n.*494C>G
|
|
ENST00000695991.1:c.541C>G
(ADA)
|
ENSP00000512314.1:p.Leu181Val
|
|
ENST00000695992.1:c.*146C>G
(ADA)
|
ENSP00000512315.1:n.*146C>G
|
|
ENST00000695993.1:c.1003C>G
(ADA)
|
ENSP00000512316.1:p.Leu335Val
|
|
ENST00000695994.1:c.*146C>G
(ADA)
|
ENSP00000512317.1:n.*146C>G
|
|
ENST00000695995.1:c.613C>G
(ADA)
|
ENSP00000512318.1:p.Leu205Val
|
|
ENST00000695996.1:n.1085C>G
(ADA)
|
|
|
ENST00000696003.1:n.2787C>G
(ADA)
|
|
|
ENST00000696004.1:n.1787C>G
(ADA)
|
|
|
ENST00000696005.1:c.453C>G
(ADA)
|
|
|
ENST00000696006.1:c.*146C>G
(ADA)
|
ENSP00000512325.1:n.*146C>G
|
|
ENST00000696007.1:c.930C>G
(ADA)
|
ENSP00000512326.1:n.930C>G
|
|
ENST00000696008.1:n.3357C>G
(ADA)
|
|
|
ENST00000696017.1:c.1000C>G
(ADA)
|
ENSP00000512333.1:p.Leu334Val
|
|
ENST00000696034.1:c.*146C>G
(ADA)
|
ENSP00000512343.1:n.*146C>G
|
|
ENST00000696035.1:n.1189C>G
(ADA)
|
|
|
ENST00000696036.1:n.1704C>G
(ADA)
|
|
|
ENST00000696037.1:n.2680C>G
(ADA)
|
|
|
ENST00000696038.1:c.*760C>G
(ADA)
|
ENSP00000512344.1:n.*760C>G
|
|
ENST00000696039.1:n.1367C>G
(ADA)
|
|
|
ENST00000696058.1:c.1000C>G
(ADA)
|
ENSP00000512361.1:p.Leu334Val
|
|
ENST00000696059.1:c.*948C>G
(ADA)
|
ENSP00000512362.1:n.*948C>G
|
|
ENST00000696060.1:c.1072C>G
(ADA)
|
ENSP00000512363.1:p.Leu358Val
|
|
ENST00000696061.1:c.1000C>G
(ADA)
|
ENSP00000512364.1:p.Leu334Val
|
|
ENST00000696062.1:c.1066C>G
(ADA)
|
ENSP00000512365.1:p.Leu356Val
|
|
ENST00000696063.1:c.1078C>G
(ADA)
|
ENSP00000512366.1:p.Leu360Val
|
|
ENST00000696064.1:c.850C>G
(ADA)
|
ENSP00000512367.1:p.Leu284Val
|
|
ENST00000696065.1:c.325C>G
(ADA)
|
ENSP00000512368.1:p.Leu109Val
|
|
ENST00000696072.1:n.358C>G
(ADA)
|
|
|
ENST00000696073.1:n.1314C>G
(ADA)
|
|
|
ENST00000696074.1:n.554C>G
(ADA)
|
|
|
ENST00000696075.1:c.*973C>G
(ADA)
|
ENSP00000512374.1:n.*973C>G
|
|
ENST00000696076.1:c.1072C>G
(ADA)
|
ENSP00000512375.1:p.Leu358Val
|
|
ENST00000696077.1:c.997C>G
(ADA)
|
ENSP00000512376.1:p.Leu333Val
|
|
ENST00000696078.1:c.1000C>G
(ADA)
|
ENSP00000512377.1:p.Leu334Val
|
|
ENST00000696079.1:c.1000C>G
(ADA)
|
ENSP00000512378.1:p.Leu334Val
|
|
ENST00000696080.1:c.1003C>G
(ADA)
|
ENSP00000512379.1:p.Leu335Val
|
|
ENST00000696081.1:n.1122C>G
(ADA)
|
|
|
ENST00000696082.1:c.1078C>G
(ADA)
|
ENSP00000512380.1:p.Leu360Val
|
|
ENST00000696083.1:n.1960C>G
(ADA)
|
|
|
ENST00000696084.1:n.1180C>G
(ADA)
|
|
|
ENST00000696104.1:c.*72C>G
(ADA)
|
ENSP00000512399.1:n.*72C>G
|
|
ENST00000372874.9:c.1003C>G
(ADA)
MANE Select
|
ENSP00000361965.4:p.Leu335Val
|
|
ENST00000372874.8:c.1003C>G
(ADA)
|
ENSP00000361965.4:p.Leu335Val
|
|
ENST00000372887.5:c.152-3559G>C
(PKIG)
|
ENSP00000361978.1:n.152-3559G>C
|
|
ENST00000464097.5:n.1369C>G
(ADA)
|
|
|
ENST00000492931.5:n.1163C>G
(ADA)
|
|
|
ENST00000536532.5:c.*146C>G
(ADA)
|
ENSP00000440946.1:n.*146C>G
|
|
ENST00000537820.1:c.931C>G
(ADA)
|
ENSP00000441818.1:p.Leu311Val
|
|
ENST00000539235.5:c.*387C>G
(ADA)
|
ENSP00000446464.1:n.*387C>G
|
|
NM_000022.2:c.1003C>G , LRG_16t1:c.1003C>G
(ADA)
|
NP_000013.2:p.Leu335Val
|
|
XM_005260236.2:c.931C>G
(ADA)
|
XP_005260293.1:p.Leu311Val
|
|
XM_011528478.1:c.598C>G
(ADA)
|
XP_011526780.1:p.Leu200Val
|
|
XM_011528479.1:c.598C>G
(ADA)
|
XP_011526781.1:p.Leu200Val
|
|
XR_244129.1:n.992C>G
(ADA)
|
|
|
NM_000022.3:c.1003C>G
(ADA)
|
NP_000013.2:p.Leu335Val
|
|
NM_001322050.1:c.598C>G
(ADA)
|
NP_001308979.1:p.Leu200Val
|
|
NM_001322051.1:c.931C>G
(ADA)
|
NP_001308980.1:p.Leu311Val
|
|
NR_136160.1:n.1089C>G
(ADA)
|
|
|
NM_000022.4:c.1003C>G
(ADA)
MANE Select
|
NP_000013.2:p.Leu335Val
|
|
NM_001322050.2:c.598C>G
(ADA)
|
NP_001308979.1:p.Leu200Val
|
|
NM_001322051.2:c.931C>G
(ADA)
|
NP_001308980.1:p.Leu311Val
|
|
NR_136160.2:n.1030C>G
(ADA)
|
|
|