|
ENST00000492931.6:n.705T>C
(ADA)
|
|
|
|
ENST00000536076.2:c.461T>C
(ADA)
|
ENSP00000512234.1:p.Val154Ala
|
|
|
ENST00000536532.6:c.614T>C
(ADA)
|
ENSP00000440946.1:p.Val205Ala
|
|
|
ENST00000537820.2:c.607-141T>C
(ADA)
|
ENSP00000441818.1:n.607-141T>C
|
|
|
ENST00000539235.6:c.226T>C
(ADA)
|
ENSP00000446464.1:p.Ter76Arg
|
|
|
ENST00000695889.1:c.219-141T>C
(ADA)
|
ENSP00000512240.1:n.219-141T>C
|
|
|
ENST00000695890.1:n.2417T>C
(ADA)
|
|
|
|
ENST00000695891.1:c.219-141T>C
(ADA)
|
ENSP00000512241.1:n.219-141T>C
|
|
|
ENST00000695927.1:c.692T>C
(ADA)
|
ENSP00000512270.1:p.Val231Ala
|
|
|
ENST00000695949.1:c.604-141T>C
(ADA)
|
ENSP00000512281.1:n.604-141T>C
|
|
|
ENST00000695957.1:c.*105T>C
(ADA)
|
ENSP00000512286.1:n.*105T>C
|
|
|
ENST00000695991.1:c.217-141T>C
(ADA)
|
ENSP00000512314.1:n.217-141T>C
|
|
|
ENST00000695992.1:c.614T>C
(ADA)
|
ENSP00000512315.1:p.Val205Ala
|
|
|
ENST00000695993.1:c.614T>C
(ADA)
|
ENSP00000512316.1:p.Val205Ala
|
|
|
ENST00000695994.1:c.614T>C
(ADA)
|
ENSP00000512317.1:p.Val205Ala
|
|
|
ENST00000695995.1:c.224T>C
(ADA)
|
ENSP00000512318.1:p.Val75Ala
|
|
|
ENST00000695996.1:n.685T>C
(ADA)
|
|
|
|
ENST00000696003.1:n.706T>C
(ADA)
|
|
|
|
ENST00000696004.1:n.706T>C
(ADA)
|
|
|
|
ENST00000696005.1:c.129-141T>C
(ADA)
|
|
|
|
ENST00000696006.1:c.607-141T>C
(ADA)
|
ENSP00000512325.1:n.607-141T>C
|
|
|
ENST00000696007.1:c.465T>C
(ADA)
|
ENSP00000512326.1:n.465T>C
|
|
|
ENST00000696008.1:n.2892T>C
(ADA)
|
|
|
|
ENST00000696017.1:c.611T>C
(ADA)
|
ENSP00000512333.1:p.Val204Ala
|
|
|
ENST00000696034.1:c.614T>C
(ADA)
|
ENSP00000512343.1:p.Val205Ala
|
|
|
ENST00000696035.1:n.724T>C
(ADA)
|
|
|
|
ENST00000696036.1:n.1304T>C
(ADA)
|
|
|
|
ENST00000696037.1:n.2291T>C
(ADA)
|
|
|
|
ENST00000696038.1:c.*360T>C
(ADA)
|
ENSP00000512344.1:n.*360T>C
|
|
|
ENST00000696039.1:n.902T>C
(ADA)
|
|
|
|
ENST00000696058.1:c.611T>C
(ADA)
|
ENSP00000512361.1:p.Val204Ala
|
|
|
ENST00000696059.1:c.*559T>C
(ADA)
|
ENSP00000512362.1:n.*559T>C
|
|
|
ENST00000696060.1:c.683T>C
(ADA)
|
ENSP00000512363.1:p.Val228Ala
|
|
|
ENST00000696061.1:c.611T>C
(ADA)
|
ENSP00000512364.1:p.Val204Ala
|
|
|
ENST00000696062.1:c.677T>C
(ADA)
|
ENSP00000512365.1:p.Val226Ala
|
|
|
ENST00000696063.1:c.689T>C
(ADA)
|
ENSP00000512366.1:p.Val230Ala
|
|
|
ENST00000696064.1:c.461T>C
(ADA)
|
ENSP00000512367.1:p.Val154Ala
|
|
|
ENST00000696065.1:c.66-141T>C
(ADA)
|
ENSP00000512368.1:n.66-141T>C
|
|
|
ENST00000696073.1:n.849T>C
(ADA)
|
|
|
|
ENST00000696074.1:n.230T>C
(ADA)
|
|
|
|
ENST00000696075.1:c.*584T>C
(ADA)
|
ENSP00000512374.1:n.*584T>C
|
|
|
ENST00000696076.1:c.683T>C
(ADA)
|
ENSP00000512375.1:p.Val228Ala
|
|
|
ENST00000696077.1:c.608T>C
(ADA)
|
ENSP00000512376.1:p.Val203Ala
|
|
|
ENST00000696078.1:c.611T>C
(ADA)
|
ENSP00000512377.1:p.Val204Ala
|
|
|
ENST00000696079.1:c.611T>C
(ADA)
|
ENSP00000512378.1:p.Val204Ala
|
|
|
ENST00000696080.1:c.614T>C
(ADA)
|
ENSP00000512379.1:p.Val205Ala
|
|
|
ENST00000696081.1:n.733T>C
(ADA)
|
|
|
|
ENST00000696082.1:c.689T>C
(ADA)
|
ENSP00000512380.1:p.Val230Ala
|
|
|
ENST00000696083.1:n.1495T>C
(ADA)
|
|
|
|
ENST00000696084.1:n.715T>C
(ADA)
|
|
|
|
ENST00000696104.1:c.363-141T>C
(ADA)
|
ENSP00000512399.1:n.363-141T>C
|
|
|
ENST00000696105.1:c.*155T>C
(ADA)
|
ENSP00000512400.1:n.*155T>C
|
|
|
ENST00000372874.9:c.614T>C
(ADA)
MANE Select
|
ENSP00000361965.4:p.Val205Ala
|
|
|
ENST00000372874.8:c.614T>C
(ADA)
|
ENSP00000361965.4:p.Val205Ala
|
|
|
ENST00000372887.5:c.152-862A>G
(PKIG)
|
ENSP00000361978.1:n.152-862A>G
|
|
|
ENST00000464097.5:n.288T>C
(ADA)
|
|
|
|
ENST00000492931.5:n.698T>C
(ADA)
|
|
|
|
ENST00000536532.5:c.614T>C
(ADA)
|
ENSP00000440946.1:p.Val205Ala
|
|
|
ENST00000537820.1:c.607-141T>C
(ADA)
|
ENSP00000441818.1:n.607-141T>C
|
|
|
ENST00000539235.5:c.226T>C
(ADA)
|
ENSP00000446464.1:p.Ter76Arg
|
|
|
NM_000022.2:c.614T>C , LRG_16t1:c.614T>C
(ADA)
|
NP_000013.2:p.Val205Ala
|
|
|
XM_005260236.2:c.607-141T>C
(ADA)
|
XP_005260293.1:n.607-141T>C
|
|
|
XM_011528478.1:c.209T>C
(ADA)
|
XP_011526780.1:p.Val70Ala
|
|
|
XM_011528479.1:c.209T>C
(ADA)
|
XP_011526781.1:p.Val70Ala
|
|
|
XR_244129.1:n.668T>C
(ADA)
|
|
|
|
NM_000022.3:c.614T>C
(ADA)
|
NP_000013.2:p.Val205Ala
|
|
|
NM_001322050.1:c.209T>C
(ADA)
|
NP_001308979.1:p.Val70Ala
|
|
|
NM_001322051.1:c.607-141T>C
(ADA)
|
NP_001308980.1:n.607-141T>C
|
|
|
NR_136160.1:n.765T>C
(ADA)
|
|
|
|
NM_000022.4:c.614T>C
(ADA)
MANE Select
|
NP_000013.2:p.Val205Ala
|
|
|
NM_001322050.2:c.209T>C
(ADA)
|
NP_001308979.1:p.Val70Ala
|
|
|
NM_001322051.2:c.607-141T>C
(ADA)
|
NP_001308980.1:n.607-141T>C
|
|
|
NR_136160.2:n.706T>C
(ADA)
|
|
|
