ENST00000492931.6:n.1145C>A
(ADA)
|
|
|
ENST00000536076.2:c.825C>A
(ADA)
|
ENSP00000512234.1:p.Asn275Lys
|
|
ENST00000536532.6:c.*121C>A
(ADA)
|
ENSP00000440946.1:n.*121C>A
|
|
ENST00000537820.2:c.906C>A
(ADA)
|
ENSP00000441818.1:p.Asn302Lys
|
|
ENST00000539235.6:c.*362C>A
(ADA)
|
ENSP00000446464.1:n.*362C>A
|
|
ENST00000695889.1:c.453C>A
(ADA)
|
ENSP00000512240.1:p.Asn151Lys
|
|
ENST00000695890.1:n.5089C>A
(ADA)
|
|
|
ENST00000695891.1:c.518C>A
(ADA)
|
ENSP00000512241.1:n.518C>A
|
|
ENST00000695927.1:c.1056C>A
(ADA)
|
ENSP00000512270.1:p.Asn352Lys
|
|
ENST00000695949.1:c.903C>A
(ADA)
|
ENSP00000512281.1:p.Asn301Lys
|
|
ENST00000695956.1:c.133C>A
(ADA)
|
|
|
ENST00000695957.1:c.*469C>A
(ADA)
|
ENSP00000512286.1:n.*469C>A
|
|
ENST00000695991.1:c.516C>A
(ADA)
|
ENSP00000512314.1:p.Asn172Lys
|
|
ENST00000695992.1:c.*121C>A
(ADA)
|
ENSP00000512315.1:n.*121C>A
|
|
ENST00000695993.1:c.978C>A
(ADA)
|
ENSP00000512316.1:p.Asn326Lys
|
|
ENST00000695994.1:c.*121C>A
(ADA)
|
ENSP00000512317.1:n.*121C>A
|
|
ENST00000695995.1:c.588C>A
(ADA)
|
ENSP00000512318.1:p.Asn196Lys
|
|
ENST00000695996.1:n.1060C>A
(ADA)
|
|
|
ENST00000696003.1:n.2762C>A
(ADA)
|
|
|
ENST00000696004.1:n.1762C>A
(ADA)
|
|
|
ENST00000696005.1:c.428C>A
(ADA)
|
|
|
ENST00000696006.1:c.*121C>A
(ADA)
|
ENSP00000512325.1:n.*121C>A
|
|
ENST00000696007.1:c.905C>A
(ADA)
|
ENSP00000512326.1:n.905C>A
|
|
ENST00000696008.1:n.3332C>A
(ADA)
|
|
|
ENST00000696017.1:c.975C>A
(ADA)
|
ENSP00000512333.1:p.Asn325Lys
|
|
ENST00000696034.1:c.*121C>A
(ADA)
|
ENSP00000512343.1:n.*121C>A
|
|
ENST00000696035.1:n.1164C>A
(ADA)
|
|
|
ENST00000696036.1:n.1679C>A
(ADA)
|
|
|
ENST00000696037.1:n.2655C>A
(ADA)
|
|
|
ENST00000696038.1:c.*735C>A
(ADA)
|
ENSP00000512344.1:n.*735C>A
|
|
ENST00000696039.1:n.1342C>A
(ADA)
|
|
|
ENST00000696058.1:c.975C>A
(ADA)
|
ENSP00000512361.1:p.Asn325Lys
|
|
ENST00000696059.1:c.*923C>A
(ADA)
|
ENSP00000512362.1:n.*923C>A
|
|
ENST00000696060.1:c.1047C>A
(ADA)
|
ENSP00000512363.1:p.Asn349Lys
|
|
ENST00000696061.1:c.975C>A
(ADA)
|
ENSP00000512364.1:p.Asn325Lys
|
|
ENST00000696062.1:c.1041C>A
(ADA)
|
ENSP00000512365.1:p.Asn347Lys
|
|
ENST00000696063.1:c.1053C>A
(ADA)
|
ENSP00000512366.1:p.Asn351Lys
|
|
ENST00000696064.1:c.825C>A
(ADA)
|
ENSP00000512367.1:p.Asn275Lys
|
|
ENST00000696065.1:c.300C>A
(ADA)
|
ENSP00000512368.1:p.Asn100Lys
|
|
ENST00000696072.1:n.333C>A
(ADA)
|
|
|
ENST00000696073.1:n.1289C>A
(ADA)
|
|
|
ENST00000696074.1:n.529C>A
(ADA)
|
|
|
ENST00000696075.1:c.*948C>A
(ADA)
|
ENSP00000512374.1:n.*948C>A
|
|
ENST00000696076.1:c.1047C>A
(ADA)
|
ENSP00000512375.1:p.Asn349Lys
|
|
ENST00000696077.1:c.972C>A
(ADA)
|
ENSP00000512376.1:p.Asn324Lys
|
|
ENST00000696078.1:c.975C>A
(ADA)
|
ENSP00000512377.1:p.Asn325Lys
|
|
ENST00000696079.1:c.975C>A
(ADA)
|
ENSP00000512378.1:p.Asn325Lys
|
|
ENST00000696080.1:c.978C>A
(ADA)
|
ENSP00000512379.1:p.Asn326Lys
|
|
ENST00000696081.1:n.1097C>A
(ADA)
|
|
|
ENST00000696082.1:c.1053C>A
(ADA)
|
ENSP00000512380.1:p.Asn351Lys
|
|
ENST00000696083.1:n.1935C>A
(ADA)
|
|
|
ENST00000696084.1:n.1155C>A
(ADA)
|
|
|
ENST00000696104.1:c.*47C>A
(ADA)
|
ENSP00000512399.1:n.*47C>A
|
|
ENST00000372874.9:c.978C>A
(ADA)
MANE Select
|
ENSP00000361965.4:p.Asn326Lys
|
|
ENST00000372874.8:c.978C>A
(ADA)
|
ENSP00000361965.4:p.Asn326Lys
|
|
ENST00000372887.5:c.152-3534G>T
(PKIG)
|
ENSP00000361978.1:n.152-3534G>T
|
|
ENST00000464097.5:n.1344C>A
(ADA)
|
|
|
ENST00000492931.5:n.1138C>A
(ADA)
|
|
|
ENST00000536532.5:c.*121C>A
(ADA)
|
ENSP00000440946.1:n.*121C>A
|
|
ENST00000537820.1:c.906C>A
(ADA)
|
ENSP00000441818.1:p.Asn302Lys
|
|
ENST00000539235.5:c.*362C>A
(ADA)
|
ENSP00000446464.1:n.*362C>A
|
|
NM_000022.2:c.978C>A , LRG_16t1:c.978C>A
(ADA)
|
NP_000013.2:p.Asn326Lys
|
|
XM_005260236.2:c.906C>A
(ADA)
|
XP_005260293.1:p.Asn302Lys
|
|
XM_011528478.1:c.573C>A
(ADA)
|
XP_011526780.1:p.Asn191Lys
|
|
XM_011528479.1:c.573C>A
(ADA)
|
XP_011526781.1:p.Asn191Lys
|
|
XR_244129.1:n.967C>A
(ADA)
|
|
|
NM_000022.3:c.978C>A
(ADA)
|
NP_000013.2:p.Asn326Lys
|
|
NM_001322050.1:c.573C>A
(ADA)
|
NP_001308979.1:p.Asn191Lys
|
|
NM_001322051.1:c.906C>A
(ADA)
|
NP_001308980.1:p.Asn302Lys
|
|
NR_136160.1:n.1064C>A
(ADA)
|
|
|
NM_000022.4:c.978C>A
(ADA)
MANE Select
|
NP_000013.2:p.Asn326Lys
|
|
NM_001322050.2:c.573C>A
(ADA)
|
NP_001308979.1:p.Asn191Lys
|
|
NM_001322051.2:c.906C>A
(ADA)
|
NP_001308980.1:p.Asn302Lys
|
|
NR_136160.2:n.1005C>A
(ADA)
|
|
|