ENST00000492931.6:n.740G>T
(ADA)
|
|
|
ENST00000536076.2:c.496G>T
(ADA)
|
ENSP00000512234.1:p.Glu166Ter
|
|
ENST00000536532.6:c.649G>T
(ADA)
|
ENSP00000440946.1:p.Glu217Ter
|
|
ENST00000537820.2:c.607-106G>T
(ADA)
|
ENSP00000441818.1:n.607-106G>T
|
|
ENST00000539235.6:c.*33G>T
(ADA)
|
ENSP00000446464.1:n.*33G>T
|
|
ENST00000695889.1:c.219-106G>T
(ADA)
|
ENSP00000512240.1:n.219-106G>T
|
|
ENST00000695890.1:n.2452G>T
(ADA)
|
|
|
ENST00000695891.1:c.219-106G>T
(ADA)
|
ENSP00000512241.1:n.219-106G>T
|
|
ENST00000695927.1:c.727G>T
(ADA)
|
ENSP00000512270.1:p.Glu243Ter
|
|
ENST00000695949.1:c.604-106G>T
(ADA)
|
ENSP00000512281.1:n.604-106G>T
|
|
ENST00000695957.1:c.*140G>T
(ADA)
|
ENSP00000512286.1:n.*140G>T
|
|
ENST00000695991.1:c.217-106G>T
(ADA)
|
ENSP00000512314.1:n.217-106G>T
|
|
ENST00000695992.1:c.649G>T
(ADA)
|
ENSP00000512315.1:p.Glu217Ter
|
|
ENST00000695993.1:c.649G>T
(ADA)
|
ENSP00000512316.1:p.Glu217Ter
|
|
ENST00000695994.1:c.649G>T
(ADA)
|
ENSP00000512317.1:p.Glu217Ter
|
|
ENST00000695995.1:c.259G>T
(ADA)
|
ENSP00000512318.1:p.Glu87Ter
|
|
ENST00000695996.1:n.720G>T
(ADA)
|
|
|
ENST00000696003.1:n.741G>T
(ADA)
|
|
|
ENST00000696004.1:n.741G>T
(ADA)
|
|
|
ENST00000696005.1:c.129-106G>T
(ADA)
|
|
|
ENST00000696006.1:c.607-106G>T
(ADA)
|
ENSP00000512325.1:n.607-106G>T
|
|
ENST00000696007.1:c.500G>T
(ADA)
|
ENSP00000512326.1:n.500G>T
|
|
ENST00000696008.1:n.2927G>T
(ADA)
|
|
|
ENST00000696017.1:c.646G>T
(ADA)
|
ENSP00000512333.1:p.Glu216Ter
|
|
ENST00000696034.1:c.649G>T
(ADA)
|
ENSP00000512343.1:p.Glu217Ter
|
|
ENST00000696035.1:n.759G>T
(ADA)
|
|
|
ENST00000696036.1:n.1339G>T
(ADA)
|
|
|
ENST00000696037.1:n.2326G>T
(ADA)
|
|
|
ENST00000696038.1:c.*395G>T
(ADA)
|
ENSP00000512344.1:n.*395G>T
|
|
ENST00000696039.1:n.937G>T
(ADA)
|
|
|
ENST00000696058.1:c.646G>T
(ADA)
|
ENSP00000512361.1:p.Glu216Ter
|
|
ENST00000696059.1:c.*594G>T
(ADA)
|
ENSP00000512362.1:n.*594G>T
|
|
ENST00000696060.1:c.718G>T
(ADA)
|
ENSP00000512363.1:p.Glu240Ter
|
|
ENST00000696061.1:c.646G>T
(ADA)
|
ENSP00000512364.1:p.Glu216Ter
|
|
ENST00000696062.1:c.712G>T
(ADA)
|
ENSP00000512365.1:p.Glu238Ter
|
|
ENST00000696063.1:c.724G>T
(ADA)
|
ENSP00000512366.1:p.Glu242Ter
|
|
ENST00000696064.1:c.496G>T
(ADA)
|
ENSP00000512367.1:p.Glu166Ter
|
|
ENST00000696065.1:c.66-106G>T
(ADA)
|
ENSP00000512368.1:n.66-106G>T
|
|
ENST00000696073.1:n.884G>T
(ADA)
|
|
|
ENST00000696074.1:n.265G>T
(ADA)
|
|
|
ENST00000696075.1:c.*619G>T
(ADA)
|
ENSP00000512374.1:n.*619G>T
|
|
ENST00000696076.1:c.718G>T
(ADA)
|
ENSP00000512375.1:p.Glu240Ter
|
|
ENST00000696077.1:c.643G>T
(ADA)
|
ENSP00000512376.1:p.Glu215Ter
|
|
ENST00000696078.1:c.646G>T
(ADA)
|
ENSP00000512377.1:p.Glu216Ter
|
|
ENST00000696079.1:c.646G>T
(ADA)
|
ENSP00000512378.1:p.Glu216Ter
|
|
ENST00000696080.1:c.649G>T
(ADA)
|
ENSP00000512379.1:p.Glu217Ter
|
|
ENST00000696081.1:n.768G>T
(ADA)
|
|
|
ENST00000696082.1:c.724G>T
(ADA)
|
ENSP00000512380.1:p.Glu242Ter
|
|
ENST00000696083.1:n.1530G>T
(ADA)
|
|
|
ENST00000696084.1:n.750G>T
(ADA)
|
|
|
ENST00000696104.1:c.363-106G>T
(ADA)
|
ENSP00000512399.1:n.363-106G>T
|
|
ENST00000696105.1:c.*190G>T
(ADA)
|
ENSP00000512400.1:n.*190G>T
|
|
ENST00000372874.9:c.649G>T
(ADA)
MANE Select
|
ENSP00000361965.4:p.Glu217Ter
|
|
ENST00000372874.8:c.649G>T
(ADA)
|
ENSP00000361965.4:p.Glu217Ter
|
|
ENST00000372887.5:c.152-897C>A
(PKIG)
|
ENSP00000361978.1:n.152-897C>A
|
|
ENST00000464097.5:n.323G>T
(ADA)
|
|
|
ENST00000492931.5:n.733G>T
(ADA)
|
|
|
ENST00000536532.5:c.649G>T
(ADA)
|
ENSP00000440946.1:p.Glu217Ter
|
|
ENST00000537820.1:c.607-106G>T
(ADA)
|
ENSP00000441818.1:n.607-106G>T
|
|
ENST00000539235.5:c.*33G>T
(ADA)
|
ENSP00000446464.1:n.*33G>T
|
|
NM_000022.2:c.649G>T , LRG_16t1:c.649G>T
(ADA)
|
NP_000013.2:p.Glu217Ter
|
|
XM_005260236.2:c.607-106G>T
(ADA)
|
XP_005260293.1:n.607-106G>T
|
|
XM_011528478.1:c.244G>T
(ADA)
|
XP_011526780.1:p.Glu82Ter
|
|
XM_011528479.1:c.244G>T
(ADA)
|
XP_011526781.1:p.Glu82Ter
|
|
XR_244129.1:n.703G>T
(ADA)
|
|
|
NM_000022.3:c.649G>T
(ADA)
|
NP_000013.2:p.Glu217Ter
|
|
NM_001322050.1:c.244G>T
(ADA)
|
NP_001308979.1:p.Glu82Ter
|
|
NM_001322051.1:c.607-106G>T
(ADA)
|
NP_001308980.1:n.607-106G>T
|
|
NR_136160.1:n.800G>T
(ADA)
|
|
|
NM_000022.4:c.649G>T
(ADA)
MANE Select
|
NP_000013.2:p.Glu217Ter
|
|
NM_001322050.2:c.244G>T
(ADA)
|
NP_001308979.1:p.Glu82Ter
|
|
NM_001322051.2:c.607-106G>T
(ADA)
|
NP_001308980.1:n.607-106G>T
|
|
NR_136160.2:n.741G>T
(ADA)
|
|
|