|
ENST00000492931.6:n.1153C>A
(ADA)
|
|
|
|
ENST00000536076.2:c.833C>A
(ADA)
|
ENSP00000512234.1:p.Ala278Glu
|
|
|
ENST00000536532.6:c.*129C>A
(ADA)
|
ENSP00000440946.1:n.*129C>A
|
|
|
ENST00000537820.2:c.914C>A
(ADA)
|
ENSP00000441818.1:p.Ala305Glu
|
|
|
ENST00000539235.6:c.*370C>A
(ADA)
|
ENSP00000446464.1:n.*370C>A
|
|
|
ENST00000695889.1:c.461C>A
(ADA)
|
ENSP00000512240.1:p.Ala154Glu
|
|
|
ENST00000695890.1:n.5097C>A
(ADA)
|
|
|
|
ENST00000695891.1:c.526C>A
(ADA)
|
ENSP00000512241.1:n.526C>A
|
|
|
ENST00000695927.1:c.1064C>A
(ADA)
|
ENSP00000512270.1:p.Ala355Glu
|
|
|
ENST00000695949.1:c.911C>A
(ADA)
|
ENSP00000512281.1:p.Ala304Glu
|
|
|
ENST00000695956.1:c.141C>A
(ADA)
|
|
|
|
ENST00000695957.1:c.*477C>A
(ADA)
|
ENSP00000512286.1:n.*477C>A
|
|
|
ENST00000695991.1:c.524C>A
(ADA)
|
ENSP00000512314.1:p.Ala175Glu
|
|
|
ENST00000695992.1:c.*129C>A
(ADA)
|
ENSP00000512315.1:n.*129C>A
|
|
|
ENST00000695993.1:c.986C>A
(ADA)
|
ENSP00000512316.1:p.Ala329Glu
|
|
|
ENST00000695994.1:c.*129C>A
(ADA)
|
ENSP00000512317.1:n.*129C>A
|
|
|
ENST00000695995.1:c.596C>A
(ADA)
|
ENSP00000512318.1:p.Ala199Glu
|
|
|
ENST00000695996.1:n.1068C>A
(ADA)
|
|
|
|
ENST00000696003.1:n.2770C>A
(ADA)
|
|
|
|
ENST00000696004.1:n.1770C>A
(ADA)
|
|
|
|
ENST00000696005.1:c.436C>A
(ADA)
|
|
|
|
ENST00000696006.1:c.*129C>A
(ADA)
|
ENSP00000512325.1:n.*129C>A
|
|
|
ENST00000696007.1:c.913C>A
(ADA)
|
ENSP00000512326.1:n.913C>A
|
|
|
ENST00000696008.1:n.3340C>A
(ADA)
|
|
|
|
ENST00000696017.1:c.983C>A
(ADA)
|
ENSP00000512333.1:p.Ala328Glu
|
|
|
ENST00000696034.1:c.*129C>A
(ADA)
|
ENSP00000512343.1:n.*129C>A
|
|
|
ENST00000696035.1:n.1172C>A
(ADA)
|
|
|
|
ENST00000696036.1:n.1687C>A
(ADA)
|
|
|
|
ENST00000696037.1:n.2663C>A
(ADA)
|
|
|
|
ENST00000696038.1:c.*743C>A
(ADA)
|
ENSP00000512344.1:n.*743C>A
|
|
|
ENST00000696039.1:n.1350C>A
(ADA)
|
|
|
|
ENST00000696058.1:c.983C>A
(ADA)
|
ENSP00000512361.1:p.Ala328Glu
|
|
|
ENST00000696059.1:c.*931C>A
(ADA)
|
ENSP00000512362.1:n.*931C>A
|
|
|
ENST00000696060.1:c.1055C>A
(ADA)
|
ENSP00000512363.1:p.Ala352Glu
|
|
|
ENST00000696061.1:c.983C>A
(ADA)
|
ENSP00000512364.1:p.Ala328Glu
|
|
|
ENST00000696062.1:c.1049C>A
(ADA)
|
ENSP00000512365.1:p.Ala350Glu
|
|
|
ENST00000696063.1:c.1061C>A
(ADA)
|
ENSP00000512366.1:p.Ala354Glu
|
|
|
ENST00000696064.1:c.833C>A
(ADA)
|
ENSP00000512367.1:p.Ala278Glu
|
|
|
ENST00000696065.1:c.308C>A
(ADA)
|
ENSP00000512368.1:p.Ala103Glu
|
|
|
ENST00000696072.1:n.341C>A
(ADA)
|
|
|
|
ENST00000696073.1:n.1297C>A
(ADA)
|
|
|
|
ENST00000696074.1:n.537C>A
(ADA)
|
|
|
|
ENST00000696075.1:c.*956C>A
(ADA)
|
ENSP00000512374.1:n.*956C>A
|
|
|
ENST00000696076.1:c.1055C>A
(ADA)
|
ENSP00000512375.1:p.Ala352Glu
|
|
|
ENST00000696077.1:c.980C>A
(ADA)
|
ENSP00000512376.1:p.Ala327Glu
|
|
|
ENST00000696078.1:c.983C>A
(ADA)
|
ENSP00000512377.1:p.Ala328Glu
|
|
|
ENST00000696079.1:c.983C>A
(ADA)
|
ENSP00000512378.1:p.Ala328Glu
|
|
|
ENST00000696080.1:c.986C>A
(ADA)
|
ENSP00000512379.1:p.Ala329Glu
|
|
|
ENST00000696081.1:n.1105C>A
(ADA)
|
|
|
|
ENST00000696082.1:c.1061C>A
(ADA)
|
ENSP00000512380.1:p.Ala354Glu
|
|
|
ENST00000696083.1:n.1943C>A
(ADA)
|
|
|
|
ENST00000696084.1:n.1163C>A
(ADA)
|
|
|
|
ENST00000696104.1:c.*55C>A
(ADA)
|
ENSP00000512399.1:n.*55C>A
|
|
|
ENST00000372874.9:c.986C>A
(ADA)
MANE Select
|
ENSP00000361965.4:p.Ala329Glu
|
|
|
ENST00000372874.8:c.986C>A
(ADA)
|
ENSP00000361965.4:p.Ala329Glu
|
|
|
ENST00000372887.5:c.152-3542G>T
(PKIG)
|
ENSP00000361978.1:n.152-3542G>T
|
|
|
ENST00000464097.5:n.1352C>A
(ADA)
|
|
|
|
ENST00000492931.5:n.1146C>A
(ADA)
|
|
|
|
ENST00000536532.5:c.*129C>A
(ADA)
|
ENSP00000440946.1:n.*129C>A
|
|
|
ENST00000537820.1:c.914C>A
(ADA)
|
ENSP00000441818.1:p.Ala305Glu
|
|
|
ENST00000539235.5:c.*370C>A
(ADA)
|
ENSP00000446464.1:n.*370C>A
|
|
|
NM_000022.2:c.986C>A , LRG_16t1:c.986C>A
(ADA)
|
NP_000013.2:p.Ala329Glu
|
|
|
XM_005260236.2:c.914C>A
(ADA)
|
XP_005260293.1:p.Ala305Glu
|
|
|
XM_011528478.1:c.581C>A
(ADA)
|
XP_011526780.1:p.Ala194Glu
|
|
|
XM_011528479.1:c.581C>A
(ADA)
|
XP_011526781.1:p.Ala194Glu
|
|
|
XR_244129.1:n.975C>A
(ADA)
|
|
|
|
NM_000022.3:c.986C>A
(ADA)
|
NP_000013.2:p.Ala329Glu
|
|
|
NM_001322050.1:c.581C>A
(ADA)
|
NP_001308979.1:p.Ala194Glu
|
|
|
NM_001322051.1:c.914C>A
(ADA)
|
NP_001308980.1:p.Ala305Glu
|
|
|
NR_136160.1:n.1072C>A
(ADA)
|
|
|
|
NM_000022.4:c.986C>A
(ADA)
MANE Select
|
NP_000013.2:p.Ala329Glu
|
|
|
NM_001322050.2:c.581C>A
(ADA)
|
NP_001308979.1:p.Ala194Glu
|
|
|
NM_001322051.2:c.914C>A
(ADA)
|
NP_001308980.1:p.Ala305Glu
|
|
|
NR_136160.2:n.1013C>A
(ADA)
|
|
|
