|
ENST00000264276.11:c.4865A>G
MANE Select
|
ENSP00000264276.6:p.His1622Arg
|
|
|
ENST00000439495.6:c.*1045A>G
|
ENSP00000403832.2:n.*1045A>G
|
|
|
ENST00000679409.1:c.*1570A>G
|
ENSP00000506531.1:n.*1570A>G
|
|
|
ENST00000679416.1:n.6369A>G
|
|
|
|
ENST00000679427.1:n.2536A>G
|
|
|
|
ENST00000679435.1:c.4865A>G
|
ENSP00000505218.1:p.His1622Arg
|
|
|
ENST00000679516.1:c.4865A>G
|
ENSP00000505187.1:p.His1622Arg
|
|
|
ENST00000679618.1:c.*1953A>G
|
ENSP00000506274.1:n.*1953A>G
|
|
|
ENST00000679630.1:n.6714A>G
|
|
|
|
ENST00000679635.1:n.3127A>G
|
|
|
|
ENST00000679686.1:n.4979A>G
|
|
|
|
ENST00000679701.1:n.7857A>G
|
|
|
|
ENST00000679916.1:c.*1213A>G
|
ENSP00000506172.1:n.*1213A>G
|
|
|
ENST00000680000.1:c.4865A>G
|
ENSP00000506173.1:p.His1622Arg
|
|
|
ENST00000680135.1:c.*2826A>G
|
ENSP00000506211.1:n.*2826A>G
|
|
|
ENST00000680149.1:c.*147A>G
|
ENSP00000506497.1:n.*147A>G
|
|
|
ENST00000680163.1:c.4865A>G
|
ENSP00000505092.1:p.His1622Arg
|
|
|
ENST00000680174.1:n.5556A>G
|
|
|
|
ENST00000680236.1:c.*1926A>G
|
ENSP00000506212.1:n.*1926A>G
|
|
|
ENST00000680404.1:n.380A>G
|
|
|
|
ENST00000680441.1:n.3423A>G
|
|
|
|
ENST00000680497.1:c.4967A>G
|
ENSP00000505954.1:p.His1656Arg
|
|
|
ENST00000680508.1:c.*21A>G
|
ENSP00000505749.1:n.*21A>G
|
|
|
ENST00000680569.1:c.*2808A>G
|
ENSP00000505522.1:n.*2808A>G
|
|
|
ENST00000680634.1:n.1373A>G
|
|
|
|
ENST00000680722.1:n.2665A>G
|
|
|
|
ENST00000680726.1:c.*147A>G
|
ENSP00000505505.1:n.*147A>G
|
|
|
ENST00000680759.1:c.4697A>G
|
ENSP00000505848.1:p.His1566Arg
|
|
|
ENST00000680814.1:c.4838+262A>G
|
ENSP00000505710.1:n.4838+262A>G
|
|
|
ENST00000680828.1:c.*2559A>G
|
ENSP00000505249.1:n.*2559A>G
|
|
|
ENST00000680861.1:c.4865A>G
|
ENSP00000505043.1:p.His1622Arg
|
|
|
ENST00000680927.1:c.*1045A>G
|
ENSP00000505473.1:n.*1045A>G
|
|
|
ENST00000680939.1:n.6806A>G
|
|
|
|
ENST00000681250.1:c.*1582A>G
|
ENSP00000505684.1:n.*1582A>G
|
|
|
ENST00000681256.1:c.*2880A>G
|
ENSP00000505446.1:n.*2880A>G
|
|
|
ENST00000681279.1:n.5731A>G
|
|
|
|
ENST00000681307.1:n.5978A>G
|
|
|
|
ENST00000681461.1:n.5633A>G
|
|
|
|
ENST00000681495.1:c.2402A>G
|
ENSP00000506085.1:p.His801Arg
|
|
|
ENST00000681558.1:c.2543A>G
|
ENSP00000505568.1:p.His848Arg
|
|
|
ENST00000681619.1:c.4862A>G
|
ENSP00000505071.1:p.His1621Arg
|
|
|
ENST00000681663.1:n.1771A>G
|
|
|
|
ENST00000681692.1:n.2825A>G
|
|
|
|
ENST00000681716.1:c.*2719A>G
|
ENSP00000505078.1:n.*2719A>G
|
|
|
ENST00000681768.1:c.*2529A>G
|
ENSP00000506311.1:n.*2529A>G
|
|
|
ENST00000681808.1:c.4688A>G
|
ENSP00000505219.1:p.His1563Arg
|
|
|
ENST00000264276.10:c.4865A>G
|
ENSP00000264276.6:p.His1622Arg
|
|
|
ENST00000439495.5:c.2969A>G
|
|
|
|
NM_020919.3:c.4865A>G
|
NP_065970.2:p.His1622Arg
|
|
|
XM_005246709.2:c.4862A>G
|
XP_005246766.1:p.His1621Arg
|
|
|
XM_006712654.1:c.4865A>G
|
XP_006712717.1:p.His1622Arg
|
|
|
XM_006712655.2:c.2801A>G
|
XP_006712718.1:p.His934Arg
|
|
|
XM_011511530.1:c.4526A>G
|
XP_011509832.1:p.His1509Arg
|
|
|
XR_922974.1:n.5143A>G
|
|
|
|
XM_006712654.3:c.4865A>G
|
XP_006712717.1:p.His1622Arg
|
|
|
XM_006712655.3:c.2801A>G
|
XP_006712718.1:p.His934Arg
|
|
|
XM_017004569.2:c.4862A>G
|
XP_016860058.1:p.His1621Arg
|
|
|
XM_017004572.2:c.2483A>G
|
XP_016860061.1:p.His828Arg
|
|
|
XM_024453024.1:c.4526A>G
|
XP_024308792.1:p.His1509Arg
|
|
|
XM_024453025.1:c.2798A>G
|
XP_024308793.1:p.His933Arg
|
|
|
XR_001738864.2:n.4980A>G
|
|
|
|
XR_001738865.2:n.4977A>G
|
|
|
|
XR_001738866.2:n.5143A>G
|
|
|
|
XR_001738867.2:n.5140A>G
|
|
|
|
XR_002959320.1:n.4036A>G
|
|
|
|
NM_020919.4:c.4865A>G
MANE Select
|
NP_065970.2:p.His1622Arg
|
|
