ENST00000574886.2:n.1676C>A
|
|
|
ENST00000576677.6:n.1597C>A
|
|
|
ENST00000681983.1:n.2604C>A
|
|
|
ENST00000682099.1:n.1365C>A
|
|
|
ENST00000682213.1:c.*439C>A
|
ENSP00000508166.1:n.*439C>A
|
|
ENST00000682315.1:c.782C>A
|
ENSP00000507232.1:p.Ala261Glu
|
|
ENST00000682479.1:c.2558C>A
|
ENSP00000508214.1:p.Ala853Glu
|
|
ENST00000682610.1:n.1708C>A
|
|
|
ENST00000682654.1:c.*439C>A
|
ENSP00000507412.1:n.*439C>A
|
|
ENST00000682722.1:c.2417C>A
|
ENSP00000508364.1:p.Ala806Glu
|
|
ENST00000683041.1:c.*439C>A
|
ENSP00000506994.1:n.*439C>A
|
|
ENST00000683184.1:c.*2121C>A
|
ENSP00000507757.1:n.*2121C>A
|
|
ENST00000683282.1:c.2384C>A
|
ENSP00000506913.1:p.Ala795Glu
|
|
ENST00000683444.1:c.*2045C>A
|
ENSP00000507553.1:n.*2045C>A
|
|
ENST00000683584.1:n.1291C>A
|
|
|
ENST00000683821.1:c.782C>A
|
ENSP00000507651.1:p.Ala261Glu
|
|
ENST00000683839.1:n.1922C>A
|
|
|
ENST00000684000.1:c.2552C>A
|
ENSP00000506795.1:p.Ala851Glu
|
|
ENST00000684188.1:c.2279C>A
|
ENSP00000507153.1:p.Ala760Glu
|
|
ENST00000684349.1:c.2654C>A
|
ENSP00000508067.1:p.Ala885Glu
|
|
ENST00000684361.1:c.2468C>A
|
ENSP00000507364.1:p.Ala823Glu
|
|
ENST00000684408.1:c.2111C>A
|
ENSP00000506837.1:p.Ala704Glu
|
|
ENST00000684429.1:c.2396C>A
|
ENSP00000507224.1:p.Ala799Glu
|
|
ENST00000684464.1:c.2561C>A
|
ENSP00000508333.1:p.Ala854Glu
|
|
ENST00000684544.1:c.2387C>A
|
ENSP00000507337.1:p.Ala796Glu
|
|
ENST00000684559.1:n.1223C>A
|
|
|
ENST00000684760.1:c.2735C>A
|
ENSP00000507696.1:p.Ala912Glu
|
|
ENST00000684776.1:c.*951C>A
|
ENSP00000507861.1:n.*951C>A
|
|
ENST00000355528.9:c.2468C>A
MANE Select
|
ENSP00000347719.4:p.Ala823Glu
|
|
ENST00000355528.8:c.2468C>A
|
ENSP00000347719.4:p.Ala823Glu
|
|
ENST00000539345.6:c.2468C>A
|
ENSP00000440671.2:p.Ala823Glu
|
|
ENST00000571618.5:n.646C>A
|
|
|
ENST00000571796.5:n.1126C>A
|
|
|
ENST00000574818.5:n.526C>A
|
|
|
ENST00000574886.1:n.852C>A
|
|
|
NM_005993.4:c.2468C>A
|
NP_005984.3:p.Ala823Glu
|
|
XM_005256396.3:c.2417C>A
|
XP_005256453.1:p.Ala806Glu
|
|
XM_005256399.3:c.1184C>A
|
XP_005256456.1:p.Ala395Glu
|
|
XM_005256400.3:c.782C>A
|
XP_005256457.1:p.Ala261Glu
|
|
XM_005256401.3:c.782C>A
|
XP_005256458.1:p.Ala261Glu
|
|
XM_005256402.3:c.782C>A
|
XP_005256459.1:p.Ala261Glu
|
|
XM_005256403.3:c.782C>A
|
XP_005256460.1:p.Ala261Glu
|
|
XM_005256404.3:c.782C>A
|
XP_005256461.1:p.Ala261Glu
|
|
XM_006722290.2:c.2387C>A
|
XP_006722353.1:p.Ala796Glu
|
|
XM_006722291.2:c.1172C>A
|
XP_006722354.1:p.Ala391Glu
|
|
XM_006722292.2:c.782C>A
|
XP_006722355.1:p.Ala261Glu
|
|
XM_011523589.1:c.2123C>A
|
XP_011521891.1:p.Ala708Glu
|
|
XM_011523590.1:c.2111C>A
|
XP_011521892.1:p.Ala704Glu
|
|
XM_011523591.1:c.2108C>A
|
XP_011521893.1:p.Ala703Glu
|
|
XM_011523592.1:c.2021C>A
|
XP_011521894.1:p.Ala674Glu
|
|
XM_011523593.1:c.1715C>A
|
XP_011521895.1:p.Ala572Glu
|
|
XM_011523594.1:c.1196C>A
|
XP_011521896.1:p.Ala399Glu
|
|
XM_011523595.1:c.1163C>A
|
XP_011521897.1:p.Ala388Glu
|
|
XM_011523597.1:c.929C>A
|
XP_011521899.1:p.Ala310Glu
|
|
XM_011523598.1:c.926C>A
|
XP_011521900.1:p.Ala309Glu
|
|
XM_011523599.1:c.920C>A
|
XP_011521901.1:p.Ala307Glu
|
|
XM_011523600.1:c.782C>A
|
XP_011521902.1:p.Ala261Glu
|
|
XR_430033.2:n.2576C>A
|
|
|
XM_005256396.4:c.2417C>A
|
XP_005256453.1:p.Ala806Glu
|
|
XM_005256399.5:c.1184C>A
|
XP_005256456.1:p.Ala395Glu
|
|
XM_005256404.4:c.782C>A
|
XP_005256461.1:p.Ala261Glu
|
|
XM_006722291.4:c.1172C>A
|
XP_006722354.1:p.Ala391Glu
|
|
XM_006722292.3:c.782C>A
|
XP_006722355.1:p.Ala261Glu
|
|
XM_011523589.2:c.2123C>A
|
XP_011521891.1:p.Ala708Glu
|
|
XM_011523591.2:c.2108C>A
|
XP_011521893.1:p.Ala703Glu
|
|
XM_011523593.2:c.1715C>A
|
XP_011521895.1:p.Ala572Glu
|
|
XM_011523594.2:c.1196C>A
|
XP_011521896.1:p.Ala399Glu
|
|
XM_011523595.3:c.1163C>A
|
XP_011521897.1:p.Ala388Glu
|
|
XM_011523597.2:c.929C>A
|
XP_011521899.1:p.Ala310Glu
|
|
XM_011523599.2:c.920C>A
|
XP_011521901.1:p.Ala307Glu
|
|
XM_011523600.3:c.782C>A
|
XP_011521902.1:p.Ala261Glu
|
|
XM_017024987.1:c.2279C>A
|
XP_016880476.1:p.Ala760Glu
|
|
XM_017024989.1:c.830C>A
|
XP_016880478.1:p.Ala277Glu
|
|
XM_017024990.2:c.782C>A
|
XP_016880479.1:p.Ala261Glu
|
|
XM_024450899.1:c.782C>A
|
XP_024306667.1:p.Ala261Glu
|
|
XM_024450900.1:c.782C>A
|
XP_024306668.1:p.Ala261Glu
|
|
XM_024450901.1:c.782C>A
|
XP_024306669.1:p.Ala261Glu
|
|
XM_024450902.1:c.782C>A
|
XP_024306670.1:p.Ala261Glu
|
|
XR_001752597.1:n.2576C>A
|
|
|
XR_001752598.1:n.2576C>A
|
|
|
XR_001752599.1:n.2576C>A
|
|
|
XR_001752600.1:n.2494C>A
|
|
|
NM_005993.5:c.2468C>A
MANE Select
|
NP_005984.3:p.Ala823Glu
|
|