ENST00000492931.6:n.1166T>C
(ADA)
|
|
|
ENST00000536076.2:c.846T>C
(ADA)
|
ENSP00000512234.1:p.Ser282=
|
|
ENST00000536532.6:c.*142T>C
(ADA)
|
ENSP00000440946.1:n.*142T>C
|
|
ENST00000537820.2:c.927T>C
(ADA)
|
ENSP00000441818.1:p.Ser309=
|
|
ENST00000539235.6:c.*383T>C
(ADA)
|
ENSP00000446464.1:n.*383T>C
|
|
ENST00000695889.1:c.474T>C
(ADA)
|
ENSP00000512240.1:p.Ser158=
|
|
ENST00000695890.1:n.5110T>C
(ADA)
|
|
|
ENST00000695891.1:c.539T>C
(ADA)
|
ENSP00000512241.1:n.539T>C
|
|
ENST00000695927.1:c.1077T>C
(ADA)
|
ENSP00000512270.1:p.Ser359=
|
|
ENST00000695949.1:c.924T>C
(ADA)
|
ENSP00000512281.1:p.Ser308=
|
|
ENST00000695956.1:c.154T>C
(ADA)
|
|
|
ENST00000695957.1:c.*490T>C
(ADA)
|
ENSP00000512286.1:n.*490T>C
|
|
ENST00000695991.1:c.537T>C
(ADA)
|
ENSP00000512314.1:p.Ser179=
|
|
ENST00000695992.1:c.*142T>C
(ADA)
|
ENSP00000512315.1:n.*142T>C
|
|
ENST00000695993.1:c.999T>C
(ADA)
|
ENSP00000512316.1:p.Ser333=
|
|
ENST00000695994.1:c.*142T>C
(ADA)
|
ENSP00000512317.1:n.*142T>C
|
|
ENST00000695995.1:c.609T>C
(ADA)
|
ENSP00000512318.1:p.Ser203=
|
|
ENST00000695996.1:n.1081T>C
(ADA)
|
|
|
ENST00000696003.1:n.2783T>C
(ADA)
|
|
|
ENST00000696004.1:n.1783T>C
(ADA)
|
|
|
ENST00000696005.1:c.449T>C
(ADA)
|
|
|
ENST00000696006.1:c.*142T>C
(ADA)
|
ENSP00000512325.1:n.*142T>C
|
|
ENST00000696007.1:c.926T>C
(ADA)
|
ENSP00000512326.1:n.926T>C
|
|
ENST00000696008.1:n.3353T>C
(ADA)
|
|
|
ENST00000696017.1:c.996T>C
(ADA)
|
ENSP00000512333.1:p.Ser332=
|
|
ENST00000696034.1:c.*142T>C
(ADA)
|
ENSP00000512343.1:n.*142T>C
|
|
ENST00000696035.1:n.1185T>C
(ADA)
|
|
|
ENST00000696036.1:n.1700T>C
(ADA)
|
|
|
ENST00000696037.1:n.2676T>C
(ADA)
|
|
|
ENST00000696038.1:c.*756T>C
(ADA)
|
ENSP00000512344.1:n.*756T>C
|
|
ENST00000696039.1:n.1363T>C
(ADA)
|
|
|
ENST00000696058.1:c.996T>C
(ADA)
|
ENSP00000512361.1:p.Ser332=
|
|
ENST00000696059.1:c.*944T>C
(ADA)
|
ENSP00000512362.1:n.*944T>C
|
|
ENST00000696060.1:c.1068T>C
(ADA)
|
ENSP00000512363.1:p.Ser356=
|
|
ENST00000696061.1:c.996T>C
(ADA)
|
ENSP00000512364.1:p.Ser332=
|
|
ENST00000696062.1:c.1062T>C
(ADA)
|
ENSP00000512365.1:p.Ser354=
|
|
ENST00000696063.1:c.1074T>C
(ADA)
|
ENSP00000512366.1:p.Ser358=
|
|
ENST00000696064.1:c.846T>C
(ADA)
|
ENSP00000512367.1:p.Ser282=
|
|
ENST00000696065.1:c.321T>C
(ADA)
|
ENSP00000512368.1:p.Ser107=
|
|
ENST00000696072.1:n.354T>C
(ADA)
|
|
|
ENST00000696073.1:n.1310T>C
(ADA)
|
|
|
ENST00000696074.1:n.550T>C
(ADA)
|
|
|
ENST00000696075.1:c.*969T>C
(ADA)
|
ENSP00000512374.1:n.*969T>C
|
|
ENST00000696076.1:c.1068T>C
(ADA)
|
ENSP00000512375.1:p.Ser356=
|
|
ENST00000696077.1:c.993T>C
(ADA)
|
ENSP00000512376.1:p.Ser331=
|
|
ENST00000696078.1:c.996T>C
(ADA)
|
ENSP00000512377.1:p.Ser332=
|
|
ENST00000696079.1:c.996T>C
(ADA)
|
ENSP00000512378.1:p.Ser332=
|
|
ENST00000696080.1:c.999T>C
(ADA)
|
ENSP00000512379.1:p.Ser333=
|
|
ENST00000696081.1:n.1118T>C
(ADA)
|
|
|
ENST00000696082.1:c.1074T>C
(ADA)
|
ENSP00000512380.1:p.Ser358=
|
|
ENST00000696083.1:n.1956T>C
(ADA)
|
|
|
ENST00000696084.1:n.1176T>C
(ADA)
|
|
|
ENST00000696104.1:c.*68T>C
(ADA)
|
ENSP00000512399.1:n.*68T>C
|
|
ENST00000372874.9:c.999T>C
(ADA)
MANE Select
|
ENSP00000361965.4:p.Ser333=
|
|
ENST00000372874.8:c.999T>C
(ADA)
|
ENSP00000361965.4:p.Ser333=
|
|
ENST00000372887.5:c.152-3555A>G
(PKIG)
|
ENSP00000361978.1:n.152-3555A>G
|
|
ENST00000464097.5:n.1365T>C
(ADA)
|
|
|
ENST00000492931.5:n.1159T>C
(ADA)
|
|
|
ENST00000536532.5:c.*142T>C
(ADA)
|
ENSP00000440946.1:n.*142T>C
|
|
ENST00000537820.1:c.927T>C
(ADA)
|
ENSP00000441818.1:p.Ser309=
|
|
ENST00000539235.5:c.*383T>C
(ADA)
|
ENSP00000446464.1:n.*383T>C
|
|
NM_000022.2:c.999T>C , LRG_16t1:c.999T>C
(ADA)
|
NP_000013.2:p.Ser333=
|
|
XM_005260236.2:c.927T>C
(ADA)
|
XP_005260293.1:p.Ser309=
|
|
XM_011528478.1:c.594T>C
(ADA)
|
XP_011526780.1:p.Ser198=
|
|
XM_011528479.1:c.594T>C
(ADA)
|
XP_011526781.1:p.Ser198=
|
|
XR_244129.1:n.988T>C
(ADA)
|
|
|
NM_000022.3:c.999T>C
(ADA)
|
NP_000013.2:p.Ser333=
|
|
NM_001322050.1:c.594T>C
(ADA)
|
NP_001308979.1:p.Ser198=
|
|
NM_001322051.1:c.927T>C
(ADA)
|
NP_001308980.1:p.Ser309=
|
|
NR_136160.1:n.1085T>C
(ADA)
|
|
|
NM_000022.4:c.999T>C
(ADA)
MANE Select
|
NP_000013.2:p.Ser333=
|
|
NM_001322050.2:c.594T>C
(ADA)
|
NP_001308979.1:p.Ser198=
|
|
NM_001322051.2:c.927T>C
(ADA)
|
NP_001308980.1:p.Ser309=
|
|
NR_136160.2:n.1026T>C
(ADA)
|
|
|