|
ENST00000492931.6:n.678G>T
(ADA)
|
|
|
|
ENST00000536076.2:c.434G>T
(ADA)
|
ENSP00000512234.1:p.Gly145Val
|
|
|
ENST00000536532.6:c.587G>T
(ADA)
|
ENSP00000440946.1:p.Gly196Val
|
|
|
ENST00000537820.2:c.587G>T
(ADA)
|
ENSP00000441818.1:p.Gly196Val
|
|
|
ENST00000539235.6:c.219-1143G>T
(ADA)
|
ENSP00000446464.1:n.219-1143G>T
|
|
|
ENST00000695889.1:c.219-1291G>T
(ADA)
|
ENSP00000512240.1:n.219-1291G>T
|
|
|
ENST00000695890.1:n.2390G>T
(ADA)
|
|
|
|
ENST00000695891.1:c.219-1291G>T
(ADA)
|
ENSP00000512241.1:n.219-1291G>T
|
|
|
ENST00000695927.1:c.665G>T
(ADA)
|
ENSP00000512270.1:p.Gly222Val
|
|
|
ENST00000695949.1:c.584G>T
(ADA)
|
ENSP00000512281.1:p.Gly195Val
|
|
|
ENST00000695957.1:c.*78G>T
(ADA)
|
ENSP00000512286.1:n.*78G>T
|
|
|
ENST00000695991.1:c.217-1291G>T
(ADA)
|
ENSP00000512314.1:n.217-1291G>T
|
|
|
ENST00000695992.1:c.587G>T
(ADA)
|
ENSP00000512315.1:p.Gly196Val
|
|
|
ENST00000695993.1:c.587G>T
(ADA)
|
ENSP00000512316.1:p.Gly196Val
|
|
|
ENST00000695994.1:c.587G>T
(ADA)
|
ENSP00000512317.1:p.Gly196Val
|
|
|
ENST00000695995.1:c.217-1143G>T
(ADA)
|
ENSP00000512318.1:n.217-1143G>T
|
|
|
ENST00000695996.1:n.658G>T
(ADA)
|
|
|
|
ENST00000695997.1:n.542G>T
(ADA)
|
|
|
|
ENST00000696003.1:n.679G>T
(ADA)
|
|
|
|
ENST00000696004.1:n.679G>T
(ADA)
|
|
|
|
ENST00000696005.1:c.109G>T
(ADA)
|
|
|
|
ENST00000696006.1:c.587G>T
(ADA)
|
ENSP00000512325.1:p.Gly196Val
|
|
|
ENST00000696007.1:c.438G>T
(ADA)
|
ENSP00000512326.1:n.438G>T
|
|
|
ENST00000696008.1:n.1742G>T
(ADA)
|
|
|
|
ENST00000696009.1:n.1937G>T
(ADA)
|
|
|
|
ENST00000696017.1:c.584G>T
(ADA)
|
ENSP00000512333.1:p.Gly195Val
|
|
|
ENST00000696034.1:c.587G>T
(ADA)
|
ENSP00000512343.1:p.Gly196Val
|
|
|
ENST00000696035.1:n.697G>T
(ADA)
|
|
|
|
ENST00000696036.1:n.1277G>T
(ADA)
|
|
|
|
ENST00000696037.1:n.2264G>T
(ADA)
|
|
|
|
ENST00000696038.1:c.*333G>T
(ADA)
|
ENSP00000512344.1:n.*333G>T
|
|
|
ENST00000696039.1:n.875G>T
(ADA)
|
|
|
|
ENST00000696058.1:c.587G>T
(ADA)
|
ENSP00000512361.1:p.Gly196Val
|
|
|
ENST00000696059.1:c.*532G>T
(ADA)
|
ENSP00000512362.1:n.*532G>T
|
|
|
ENST00000696060.1:c.587G>T
(ADA)
|
ENSP00000512363.1:p.Gly196Val
|
|
|
ENST00000696061.1:c.584G>T
(ADA)
|
ENSP00000512364.1:p.Gly195Val
|
|
|
ENST00000696062.1:c.650G>T
(ADA)
|
ENSP00000512365.1:p.Gly217Val
|
|
|
ENST00000696063.1:c.662G>T
(ADA)
|
ENSP00000512366.1:p.Gly221Val
|
|
|
ENST00000696064.1:c.434G>T
(ADA)
|
ENSP00000512367.1:p.Gly145Val
|
|
|
ENST00000696065.1:c.66-1291G>T
(ADA)
|
ENSP00000512368.1:n.66-1291G>T
|
|
|
ENST00000696074.1:n.203G>T
(ADA)
|
|
|
|
ENST00000696075.1:c.*557G>T
(ADA)
|
ENSP00000512374.1:n.*557G>T
|
|
|
ENST00000696076.1:c.587G>T
(ADA)
|
ENSP00000512375.1:p.Gly196Val
|
|
|
ENST00000696077.1:c.584G>T
(ADA)
|
ENSP00000512376.1:p.Gly195Val
|
|
|
ENST00000696078.1:c.587G>T
(ADA)
|
ENSP00000512377.1:p.Gly196Val
|
|
|
ENST00000696079.1:c.587G>T
(ADA)
|
ENSP00000512378.1:p.Gly196Val
|
|
|
ENST00000696080.1:c.587G>T
(ADA)
|
ENSP00000512379.1:p.Gly196Val
|
|
|
ENST00000696081.1:n.706G>T
(ADA)
|
|
|
|
ENST00000696082.1:c.665G>T
(ADA)
|
ENSP00000512380.1:p.Gly222Val
|
|
|
ENST00000696083.1:n.1468G>T
(ADA)
|
|
|
|
ENST00000696084.1:n.688G>T
(ADA)
|
|
|
|
ENST00000696104.1:c.363-1291G>T
(ADA)
|
ENSP00000512399.1:n.363-1291G>T
|
|
|
ENST00000696105.1:c.*128G>T
(ADA)
|
ENSP00000512400.1:n.*128G>T
|
|
|
ENST00000372874.9:c.587G>T
(ADA)
MANE Select
|
ENSP00000361965.4:p.Gly196Val
|
|
|
ENST00000372874.8:c.587G>T
(ADA)
|
ENSP00000361965.4:p.Gly196Val
|
|
|
ENST00000372887.5:c.*245C>A
(PKIG)
|
ENSP00000361978.1:n.*245C>A
|
|
|
ENST00000464097.5:n.261G>T
(ADA)
|
|
|
|
ENST00000492931.5:n.671G>T
(ADA)
|
|
|
|
ENST00000536532.5:c.587G>T
(ADA)
|
ENSP00000440946.1:p.Gly196Val
|
|
|
ENST00000537820.1:c.587G>T
(ADA)
|
ENSP00000441818.1:p.Gly196Val
|
|
|
ENST00000539235.5:c.219-1143G>T
(ADA)
|
ENSP00000446464.1:n.219-1143G>T
|
|
|
NM_000022.2:c.587G>T , LRG_16t1:c.587G>T
(ADA)
|
NP_000013.2:p.Gly196Val
|
|
|
XM_005260236.2:c.587G>T
(ADA)
|
XP_005260293.1:p.Gly196Val
|
|
|
XM_011528478.1:c.182G>T
(ADA)
|
XP_011526780.1:p.Gly61Val
|
|
|
XM_011528479.1:c.182G>T
(ADA)
|
XP_011526781.1:p.Gly61Val
|
|
|
XR_244129.1:n.641G>T
(ADA)
|
|
|
|
NM_000022.3:c.587G>T
(ADA)
|
NP_000013.2:p.Gly196Val
|
|
|
NM_001322050.1:c.182G>T
(ADA)
|
NP_001308979.1:p.Gly61Val
|
|
|
NM_001322051.1:c.587G>T
(ADA)
|
NP_001308980.1:p.Gly196Val
|
|
|
NR_136160.1:n.738G>T
(ADA)
|
|
|
|
NM_000022.4:c.587G>T
(ADA)
MANE Select
|
NP_000013.2:p.Gly196Val
|
|
|
NM_001322050.2:c.182G>T
(ADA)
|
NP_001308979.1:p.Gly61Val
|
|
|
NM_001322051.2:c.587G>T
(ADA)
|
NP_001308980.1:p.Gly196Val
|
|
|
NR_136160.2:n.679G>T
(ADA)
|
|
|
