ENST00000492931.6:n.715C>T
(ADA)
|
|
|
ENST00000536076.2:c.471C>T
(ADA)
|
ENSP00000512234.1:p.Gly157=
|
|
ENST00000536532.6:c.624C>T
(ADA)
|
ENSP00000440946.1:p.Gly208=
|
|
ENST00000537820.2:c.607-131C>T
(ADA)
|
ENSP00000441818.1:n.607-131C>T
|
|
ENST00000539235.6:c.*8C>T
(ADA)
|
ENSP00000446464.1:n.*8C>T
|
|
ENST00000695889.1:c.219-131C>T
(ADA)
|
ENSP00000512240.1:n.219-131C>T
|
|
ENST00000695890.1:n.2427C>T
(ADA)
|
|
|
ENST00000695891.1:c.219-131C>T
(ADA)
|
ENSP00000512241.1:n.219-131C>T
|
|
ENST00000695927.1:c.702C>T
(ADA)
|
ENSP00000512270.1:p.Gly234=
|
|
ENST00000695949.1:c.604-131C>T
(ADA)
|
ENSP00000512281.1:n.604-131C>T
|
|
ENST00000695957.1:c.*115C>T
(ADA)
|
ENSP00000512286.1:n.*115C>T
|
|
ENST00000695991.1:c.217-131C>T
(ADA)
|
ENSP00000512314.1:n.217-131C>T
|
|
ENST00000695992.1:c.624C>T
(ADA)
|
ENSP00000512315.1:p.Gly208=
|
|
ENST00000695993.1:c.624C>T
(ADA)
|
ENSP00000512316.1:p.Gly208=
|
|
ENST00000695994.1:c.624C>T
(ADA)
|
ENSP00000512317.1:p.Gly208=
|
|
ENST00000695995.1:c.234C>T
(ADA)
|
ENSP00000512318.1:p.Gly78=
|
|
ENST00000695996.1:n.695C>T
(ADA)
|
|
|
ENST00000696003.1:n.716C>T
(ADA)
|
|
|
ENST00000696004.1:n.716C>T
(ADA)
|
|
|
ENST00000696005.1:c.129-131C>T
(ADA)
|
|
|
ENST00000696006.1:c.607-131C>T
(ADA)
|
ENSP00000512325.1:n.607-131C>T
|
|
ENST00000696007.1:c.475C>T
(ADA)
|
ENSP00000512326.1:n.475C>T
|
|
ENST00000696008.1:n.2902C>T
(ADA)
|
|
|
ENST00000696017.1:c.621C>T
(ADA)
|
ENSP00000512333.1:p.Gly207=
|
|
ENST00000696034.1:c.624C>T
(ADA)
|
ENSP00000512343.1:p.Gly208=
|
|
ENST00000696035.1:n.734C>T
(ADA)
|
|
|
ENST00000696036.1:n.1314C>T
(ADA)
|
|
|
ENST00000696037.1:n.2301C>T
(ADA)
|
|
|
ENST00000696038.1:c.*370C>T
(ADA)
|
ENSP00000512344.1:n.*370C>T
|
|
ENST00000696039.1:n.912C>T
(ADA)
|
|
|
ENST00000696058.1:c.621C>T
(ADA)
|
ENSP00000512361.1:p.Gly207=
|
|
ENST00000696059.1:c.*569C>T
(ADA)
|
ENSP00000512362.1:n.*569C>T
|
|
ENST00000696060.1:c.693C>T
(ADA)
|
ENSP00000512363.1:p.Gly231=
|
|
ENST00000696061.1:c.621C>T
(ADA)
|
ENSP00000512364.1:p.Gly207=
|
|
ENST00000696062.1:c.687C>T
(ADA)
|
ENSP00000512365.1:p.Gly229=
|
|
ENST00000696063.1:c.699C>T
(ADA)
|
ENSP00000512366.1:p.Gly233=
|
|
ENST00000696064.1:c.471C>T
(ADA)
|
ENSP00000512367.1:p.Gly157=
|
|
ENST00000696065.1:c.66-131C>T
(ADA)
|
ENSP00000512368.1:n.66-131C>T
|
|
ENST00000696073.1:n.859C>T
(ADA)
|
|
|
ENST00000696074.1:n.240C>T
(ADA)
|
|
|
ENST00000696075.1:c.*594C>T
(ADA)
|
ENSP00000512374.1:n.*594C>T
|
|
ENST00000696076.1:c.693C>T
(ADA)
|
ENSP00000512375.1:p.Gly231=
|
|
ENST00000696077.1:c.618C>T
(ADA)
|
ENSP00000512376.1:p.Gly206=
|
|
ENST00000696078.1:c.621C>T
(ADA)
|
ENSP00000512377.1:p.Gly207=
|
|
ENST00000696079.1:c.621C>T
(ADA)
|
ENSP00000512378.1:p.Gly207=
|
|
ENST00000696080.1:c.624C>T
(ADA)
|
ENSP00000512379.1:p.Gly208=
|
|
ENST00000696081.1:n.743C>T
(ADA)
|
|
|
ENST00000696082.1:c.699C>T
(ADA)
|
ENSP00000512380.1:p.Gly233=
|
|
ENST00000696083.1:n.1505C>T
(ADA)
|
|
|
ENST00000696084.1:n.725C>T
(ADA)
|
|
|
ENST00000696104.1:c.363-131C>T
(ADA)
|
ENSP00000512399.1:n.363-131C>T
|
|
ENST00000696105.1:c.*165C>T
(ADA)
|
ENSP00000512400.1:n.*165C>T
|
|
ENST00000372874.9:c.624C>T
(ADA)
MANE Select
|
ENSP00000361965.4:p.Gly208=
|
|
ENST00000372874.8:c.624C>T
(ADA)
|
ENSP00000361965.4:p.Gly208=
|
|
ENST00000372887.5:c.152-872G>A
(PKIG)
|
ENSP00000361978.1:n.152-872G>A
|
|
ENST00000464097.5:n.298C>T
(ADA)
|
|
|
ENST00000492931.5:n.708C>T
(ADA)
|
|
|
ENST00000536532.5:c.624C>T
(ADA)
|
ENSP00000440946.1:p.Gly208=
|
|
ENST00000537820.1:c.607-131C>T
(ADA)
|
ENSP00000441818.1:n.607-131C>T
|
|
ENST00000539235.5:c.*8C>T
(ADA)
|
ENSP00000446464.1:n.*8C>T
|
|
NM_000022.2:c.624C>T , LRG_16t1:c.624C>T
(ADA)
|
NP_000013.2:p.Gly208=
|
|
XM_005260236.2:c.607-131C>T
(ADA)
|
XP_005260293.1:n.607-131C>T
|
|
XM_011528478.1:c.219C>T
(ADA)
|
XP_011526780.1:p.Gly73=
|
|
XM_011528479.1:c.219C>T
(ADA)
|
XP_011526781.1:p.Gly73=
|
|
XR_244129.1:n.678C>T
(ADA)
|
|
|
NM_000022.3:c.624C>T
(ADA)
|
NP_000013.2:p.Gly208=
|
|
NM_001322050.1:c.219C>T
(ADA)
|
NP_001308979.1:p.Gly73=
|
|
NM_001322051.1:c.607-131C>T
(ADA)
|
NP_001308980.1:n.607-131C>T
|
|
NR_136160.1:n.775C>T
(ADA)
|
|
|
NM_000022.4:c.624C>T
(ADA)
MANE Select
|
NP_000013.2:p.Gly208=
|
|
NM_001322050.2:c.219C>T
(ADA)
|
NP_001308979.1:p.Gly73=
|
|
NM_001322051.2:c.607-131C>T
(ADA)
|
NP_001308980.1:n.607-131C>T
|
|
NR_136160.2:n.716C>T
(ADA)
|
|
|