|
ENST00000264276.11:c.4853G>A
MANE Select
|
ENSP00000264276.6:p.Gly1618Asp
|
|
|
ENST00000439495.6:c.*1033G>A
|
ENSP00000403832.2:n.*1033G>A
|
|
|
ENST00000679409.1:c.*1558G>A
|
ENSP00000506531.1:n.*1558G>A
|
|
|
ENST00000679416.1:n.6357G>A
|
|
|
|
ENST00000679427.1:n.2524G>A
|
|
|
|
ENST00000679435.1:c.4853G>A
|
ENSP00000505218.1:p.Gly1618Asp
|
|
|
ENST00000679516.1:c.4853G>A
|
ENSP00000505187.1:p.Gly1618Asp
|
|
|
ENST00000679618.1:c.*1941G>A
|
ENSP00000506274.1:n.*1941G>A
|
|
|
ENST00000679630.1:n.6702G>A
|
|
|
|
ENST00000679635.1:n.3115G>A
|
|
|
|
ENST00000679686.1:n.4967G>A
|
|
|
|
ENST00000679701.1:n.7845G>A
|
|
|
|
ENST00000679916.1:c.*1201G>A
|
ENSP00000506172.1:n.*1201G>A
|
|
|
ENST00000680000.1:c.4853G>A
|
ENSP00000506173.1:p.Gly1618Asp
|
|
|
ENST00000680135.1:c.*2814G>A
|
ENSP00000506211.1:n.*2814G>A
|
|
|
ENST00000680149.1:c.*135G>A
|
ENSP00000506497.1:n.*135G>A
|
|
|
ENST00000680163.1:c.4853G>A
|
ENSP00000505092.1:p.Gly1618Asp
|
|
|
ENST00000680174.1:n.5544G>A
|
|
|
|
ENST00000680236.1:c.*1914G>A
|
ENSP00000506212.1:n.*1914G>A
|
|
|
ENST00000680404.1:n.368G>A
|
|
|
|
ENST00000680441.1:n.3411G>A
|
|
|
|
ENST00000680497.1:c.4955G>A
|
ENSP00000505954.1:p.Gly1652Asp
|
|
|
ENST00000680508.1:c.*9G>A
|
ENSP00000505749.1:n.*9G>A
|
|
|
ENST00000680569.1:c.*2796G>A
|
ENSP00000505522.1:n.*2796G>A
|
|
|
ENST00000680634.1:n.1361G>A
|
|
|
|
ENST00000680722.1:n.2653G>A
|
|
|
|
ENST00000680726.1:c.*135G>A
|
ENSP00000505505.1:n.*135G>A
|
|
|
ENST00000680759.1:c.4685G>A
|
ENSP00000505848.1:p.Gly1562Asp
|
|
|
ENST00000680814.1:c.4838+250G>A
|
ENSP00000505710.1:n.4838+250G>A
|
|
|
ENST00000680828.1:c.*2547G>A
|
ENSP00000505249.1:n.*2547G>A
|
|
|
ENST00000680861.1:c.4853G>A
|
ENSP00000505043.1:p.Gly1618Asp
|
|
|
ENST00000680927.1:c.*1033G>A
|
ENSP00000505473.1:n.*1033G>A
|
|
|
ENST00000680939.1:n.6794G>A
|
|
|
|
ENST00000681250.1:c.*1570G>A
|
ENSP00000505684.1:n.*1570G>A
|
|
|
ENST00000681256.1:c.*2868G>A
|
ENSP00000505446.1:n.*2868G>A
|
|
|
ENST00000681279.1:n.5719G>A
|
|
|
|
ENST00000681307.1:n.5966G>A
|
|
|
|
ENST00000681461.1:n.5621G>A
|
|
|
|
ENST00000681495.1:c.2390G>A
|
ENSP00000506085.1:p.Gly797Asp
|
|
|
ENST00000681558.1:c.2531G>A
|
ENSP00000505568.1:p.Gly844Asp
|
|
|
ENST00000681619.1:c.4850G>A
|
ENSP00000505071.1:p.Gly1617Asp
|
|
|
ENST00000681663.1:n.1759G>A
|
|
|
|
ENST00000681692.1:n.2813G>A
|
|
|
|
ENST00000681716.1:c.*2707G>A
|
ENSP00000505078.1:n.*2707G>A
|
|
|
ENST00000681768.1:c.*2517G>A
|
ENSP00000506311.1:n.*2517G>A
|
|
|
ENST00000681808.1:c.4676G>A
|
ENSP00000505219.1:p.Gly1559Asp
|
|
|
ENST00000264276.10:c.4853G>A
|
ENSP00000264276.6:p.Gly1618Asp
|
|
|
ENST00000439495.5:c.2957G>A
|
|
|
|
NM_020919.3:c.4853G>A
|
NP_065970.2:p.Gly1618Asp
|
|
|
XM_005246709.2:c.4850G>A
|
XP_005246766.1:p.Gly1617Asp
|
|
|
XM_006712654.1:c.4853G>A
|
XP_006712717.1:p.Gly1618Asp
|
|
|
XM_006712655.2:c.2789G>A
|
XP_006712718.1:p.Gly930Asp
|
|
|
XM_011511530.1:c.4514G>A
|
XP_011509832.1:p.Gly1505Asp
|
|
|
XR_922974.1:n.5131G>A
|
|
|
|
XM_006712654.3:c.4853G>A
|
XP_006712717.1:p.Gly1618Asp
|
|
|
XM_006712655.3:c.2789G>A
|
XP_006712718.1:p.Gly930Asp
|
|
|
XM_017004569.2:c.4850G>A
|
XP_016860058.1:p.Gly1617Asp
|
|
|
XM_017004572.2:c.2471G>A
|
XP_016860061.1:p.Gly824Asp
|
|
|
XM_024453024.1:c.4514G>A
|
XP_024308792.1:p.Gly1505Asp
|
|
|
XM_024453025.1:c.2786G>A
|
XP_024308793.1:p.Gly929Asp
|
|
|
XR_001738864.2:n.4968G>A
|
|
|
|
XR_001738865.2:n.4965G>A
|
|
|
|
XR_001738866.2:n.5131G>A
|
|
|
|
XR_001738867.2:n.5128G>A
|
|
|
|
XR_002959320.1:n.4024G>A
|
|
|
|
NM_020919.4:c.4853G>A
MANE Select
|
NP_065970.2:p.Gly1618Asp
|
|
