ENST00000492931.6:n.881C>T
(ADA)
|
|
|
ENST00000536076.2:c.561C>T
(ADA)
|
ENSP00000512234.1:p.His187=
|
|
ENST00000536532.6:c.714C>T
(ADA)
|
ENSP00000440946.1:p.His238=
|
|
ENST00000537820.2:c.642C>T
(ADA)
|
ENSP00000441818.1:p.His214=
|
|
ENST00000539235.6:c.*98C>T
(ADA)
|
ENSP00000446464.1:n.*98C>T
|
|
ENST00000695889.1:c.254C>T
(ADA)
|
ENSP00000512240.1:p.Thr85Met
|
|
ENST00000695890.1:n.2593C>T
(ADA)
|
|
|
ENST00000695891.1:c.254C>T
(ADA)
|
ENSP00000512241.1:p.Thr85Met
|
|
ENST00000695927.1:c.792C>T
(ADA)
|
ENSP00000512270.1:p.His264=
|
|
ENST00000695949.1:c.639C>T
(ADA)
|
ENSP00000512281.1:p.His213=
|
|
ENST00000695957.1:c.*205C>T
(ADA)
|
ENSP00000512286.1:n.*205C>T
|
|
ENST00000695991.1:c.252C>T
(ADA)
|
ENSP00000512314.1:p.His84=
|
|
ENST00000695992.1:c.714C>T
(ADA)
|
ENSP00000512315.1:p.His238=
|
|
ENST00000695993.1:c.714C>T
(ADA)
|
ENSP00000512316.1:p.His238=
|
|
ENST00000695994.1:c.687C>T
(ADA)
|
ENSP00000512317.1:p.His229=
|
|
ENST00000695995.1:c.324C>T
(ADA)
|
ENSP00000512318.1:p.His108=
|
|
ENST00000695996.1:n.861C>T
(ADA)
|
|
|
ENST00000696003.1:n.882C>T
(ADA)
|
|
|
ENST00000696004.1:n.882C>T
(ADA)
|
|
|
ENST00000696005.1:c.164C>T
(ADA)
|
|
|
ENST00000696006.1:c.642C>T
(ADA)
|
ENSP00000512325.1:p.His214=
|
|
ENST00000696007.1:c.641C>T
(ADA)
|
ENSP00000512326.1:n.641C>T
|
|
ENST00000696008.1:n.3068C>T
(ADA)
|
|
|
ENST00000696017.1:c.711C>T
(ADA)
|
ENSP00000512333.1:p.His237=
|
|
ENST00000696034.1:c.714C>T
(ADA)
|
ENSP00000512343.1:p.His238=
|
|
ENST00000696035.1:n.900C>T
(ADA)
|
|
|
ENST00000696036.1:n.1480C>T
(ADA)
|
|
|
ENST00000696037.1:n.2391C>T
(ADA)
|
|
|
ENST00000696038.1:c.*536C>T
(ADA)
|
ENSP00000512344.1:n.*536C>T
|
|
ENST00000696039.1:n.1078C>T
(ADA)
|
|
|
ENST00000696058.1:c.711C>T
(ADA)
|
ENSP00000512361.1:p.His237=
|
|
ENST00000696059.1:c.*659C>T
(ADA)
|
ENSP00000512362.1:n.*659C>T
|
|
ENST00000696060.1:c.783C>T
(ADA)
|
ENSP00000512363.1:p.His261=
|
|
ENST00000696061.1:c.711C>T
(ADA)
|
ENSP00000512364.1:p.His237=
|
|
ENST00000696062.1:c.777C>T
(ADA)
|
ENSP00000512365.1:p.His259=
|
|
ENST00000696063.1:c.789C>T
(ADA)
|
ENSP00000512366.1:p.His263=
|
|
ENST00000696064.1:c.561C>T
(ADA)
|
ENSP00000512367.1:p.His187=
|
|
ENST00000696065.1:c.101C>T
(ADA)
|
ENSP00000512368.1:p.Thr34Met
|
|
ENST00000696073.1:n.1025C>T
(ADA)
|
|
|
ENST00000696074.1:n.330C>T
(ADA)
|
|
|
ENST00000696075.1:c.*684C>T
(ADA)
|
ENSP00000512374.1:n.*684C>T
|
|
ENST00000696076.1:c.783C>T
(ADA)
|
ENSP00000512375.1:p.His261=
|
|
ENST00000696077.1:c.708C>T
(ADA)
|
ENSP00000512376.1:p.His236=
|
|
ENST00000696078.1:c.711C>T
(ADA)
|
ENSP00000512377.1:p.His237=
|
|
ENST00000696079.1:c.711C>T
(ADA)
|
ENSP00000512378.1:p.His237=
|
|
ENST00000696080.1:c.714C>T
(ADA)
|
ENSP00000512379.1:p.His238=
|
|
ENST00000696081.1:n.833C>T
(ADA)
|
|
|
ENST00000696082.1:c.789C>T
(ADA)
|
ENSP00000512380.1:p.His263=
|
|
ENST00000696083.1:n.1671C>T
(ADA)
|
|
|
ENST00000696084.1:n.891C>T
(ADA)
|
|
|
ENST00000696104.1:c.398C>T
(ADA)
|
ENSP00000512399.1:p.Thr133Met
|
|
ENST00000372874.9:c.714C>T
(ADA)
MANE Select
|
ENSP00000361965.4:p.His238=
|
|
ENST00000372874.8:c.714C>T
(ADA)
|
ENSP00000361965.4:p.His238=
|
|
ENST00000372887.5:c.152-1038G>A
(PKIG)
|
ENSP00000361978.1:n.152-1038G>A
|
|
ENST00000464097.5:n.464C>T
(ADA)
|
|
|
ENST00000492931.5:n.874C>T
(ADA)
|
|
|
ENST00000536532.5:c.714C>T
(ADA)
|
ENSP00000440946.1:p.His238=
|
|
ENST00000537820.1:c.642C>T
(ADA)
|
ENSP00000441818.1:p.His214=
|
|
ENST00000539235.5:c.*98C>T
(ADA)
|
ENSP00000446464.1:n.*98C>T
|
|
NM_000022.2:c.714C>T , LRG_16t1:c.714C>T
(ADA)
|
NP_000013.2:p.His238=
|
|
XM_005260236.2:c.642C>T
(ADA)
|
XP_005260293.1:p.His214=
|
|
XM_011528478.1:c.309C>T
(ADA)
|
XP_011526780.1:p.His103=
|
|
XM_011528479.1:c.309C>T
(ADA)
|
XP_011526781.1:p.His103=
|
|
XR_244129.1:n.768C>T
(ADA)
|
|
|
NM_000022.3:c.714C>T
(ADA)
|
NP_000013.2:p.His238=
|
|
NM_001322050.1:c.309C>T
(ADA)
|
NP_001308979.1:p.His103=
|
|
NM_001322051.1:c.642C>T
(ADA)
|
NP_001308980.1:p.His214=
|
|
NR_136160.1:n.865C>T
(ADA)
|
|
|
NM_000022.4:c.714C>T
(ADA)
MANE Select
|
NP_000013.2:p.His238=
|
|
NM_001322050.2:c.309C>T
(ADA)
|
NP_001308979.1:p.His103=
|
|
NM_001322051.2:c.642C>T
(ADA)
|
NP_001308980.1:p.His214=
|
|
NR_136160.2:n.806C>T
(ADA)
|
|
|