|
ENST00000264276.11:c.4844G>A
MANE Select
|
ENSP00000264276.6:p.Arg1615Lys
|
|
|
ENST00000439495.6:c.*1024G>A
|
ENSP00000403832.2:n.*1024G>A
|
|
|
ENST00000679409.1:c.*1549G>A
|
ENSP00000506531.1:n.*1549G>A
|
|
|
ENST00000679416.1:n.6348G>A
|
|
|
|
ENST00000679427.1:n.2515G>A
|
|
|
|
ENST00000679435.1:c.4844G>A
|
ENSP00000505218.1:p.Arg1615Lys
|
|
|
ENST00000679516.1:c.4844G>A
|
ENSP00000505187.1:p.Arg1615Lys
|
|
|
ENST00000679618.1:c.*1932G>A
|
ENSP00000506274.1:n.*1932G>A
|
|
|
ENST00000679630.1:n.6693G>A
|
|
|
|
ENST00000679635.1:n.3106G>A
|
|
|
|
ENST00000679686.1:n.4958G>A
|
|
|
|
ENST00000679701.1:n.7836G>A
|
|
|
|
ENST00000679916.1:c.*1192G>A
|
ENSP00000506172.1:n.*1192G>A
|
|
|
ENST00000680000.1:c.4844G>A
|
ENSP00000506173.1:p.Arg1615Lys
|
|
|
ENST00000680135.1:c.*2805G>A
|
ENSP00000506211.1:n.*2805G>A
|
|
|
ENST00000680149.1:c.*126G>A
|
ENSP00000506497.1:n.*126G>A
|
|
|
ENST00000680163.1:c.4844G>A
|
ENSP00000505092.1:p.Arg1615Lys
|
|
|
ENST00000680174.1:n.5535G>A
|
|
|
|
ENST00000680236.1:c.*1905G>A
|
ENSP00000506212.1:n.*1905G>A
|
|
|
ENST00000680404.1:n.359G>A
|
|
|
|
ENST00000680441.1:n.3402G>A
|
|
|
|
ENST00000680497.1:c.4946G>A
|
ENSP00000505954.1:p.Arg1649Lys
|
|
|
ENST00000680508.1:c.4863G>A
|
ENSP00000505749.1:p.Ter1621=
|
|
|
ENST00000680569.1:c.*2787G>A
|
ENSP00000505522.1:n.*2787G>A
|
|
|
ENST00000680634.1:n.1352G>A
|
|
|
|
ENST00000680722.1:n.2644G>A
|
|
|
|
ENST00000680726.1:c.*126G>A
|
ENSP00000505505.1:n.*126G>A
|
|
|
ENST00000680759.1:c.4676G>A
|
ENSP00000505848.1:p.Arg1559Lys
|
|
|
ENST00000680814.1:c.4838+241G>A
|
ENSP00000505710.1:n.4838+241G>A
|
|
|
ENST00000680828.1:c.*2538G>A
|
ENSP00000505249.1:n.*2538G>A
|
|
|
ENST00000680861.1:c.4844G>A
|
ENSP00000505043.1:p.Arg1615Lys
|
|
|
ENST00000680927.1:c.*1024G>A
|
ENSP00000505473.1:n.*1024G>A
|
|
|
ENST00000680939.1:n.6785G>A
|
|
|
|
ENST00000681250.1:c.*1561G>A
|
ENSP00000505684.1:n.*1561G>A
|
|
|
ENST00000681256.1:c.*2859G>A
|
ENSP00000505446.1:n.*2859G>A
|
|
|
ENST00000681279.1:n.5710G>A
|
|
|
|
ENST00000681307.1:n.5957G>A
|
|
|
|
ENST00000681461.1:n.5612G>A
|
|
|
|
ENST00000681495.1:c.2381G>A
|
ENSP00000506085.1:p.Arg794Lys
|
|
|
ENST00000681558.1:c.2522G>A
|
ENSP00000505568.1:p.Arg841Lys
|
|
|
ENST00000681619.1:c.4841G>A
|
ENSP00000505071.1:p.Arg1614Lys
|
|
|
ENST00000681663.1:n.1750G>A
|
|
|
|
ENST00000681692.1:n.2804G>A
|
|
|
|
ENST00000681716.1:c.*2698G>A
|
ENSP00000505078.1:n.*2698G>A
|
|
|
ENST00000681768.1:c.*2508G>A
|
ENSP00000506311.1:n.*2508G>A
|
|
|
ENST00000681808.1:c.4667G>A
|
ENSP00000505219.1:p.Arg1556Lys
|
|
|
ENST00000264276.10:c.4844G>A
|
ENSP00000264276.6:p.Arg1615Lys
|
|
|
ENST00000439495.5:c.2948G>A
|
|
|
|
NM_020919.3:c.4844G>A
|
NP_065970.2:p.Arg1615Lys
|
|
|
XM_005246709.2:c.4841G>A
|
XP_005246766.1:p.Arg1614Lys
|
|
|
XM_006712654.1:c.4844G>A
|
XP_006712717.1:p.Arg1615Lys
|
|
|
XM_006712655.2:c.2780G>A
|
XP_006712718.1:p.Arg927Lys
|
|
|
XM_011511530.1:c.4505G>A
|
XP_011509832.1:p.Arg1502Lys
|
|
|
XR_922974.1:n.5122G>A
|
|
|
|
XM_006712654.3:c.4844G>A
|
XP_006712717.1:p.Arg1615Lys
|
|
|
XM_006712655.3:c.2780G>A
|
XP_006712718.1:p.Arg927Lys
|
|
|
XM_017004569.2:c.4841G>A
|
XP_016860058.1:p.Arg1614Lys
|
|
|
XM_017004572.2:c.2462G>A
|
XP_016860061.1:p.Arg821Lys
|
|
|
XM_024453024.1:c.4505G>A
|
XP_024308792.1:p.Arg1502Lys
|
|
|
XM_024453025.1:c.2777G>A
|
XP_024308793.1:p.Arg926Lys
|
|
|
XR_001738864.2:n.4959G>A
|
|
|
|
XR_001738865.2:n.4956G>A
|
|
|
|
XR_001738866.2:n.5122G>A
|
|
|
|
XR_001738867.2:n.5119G>A
|
|
|
|
XR_002959320.1:n.4015G>A
|
|
|
|
NM_020919.4:c.4844G>A
MANE Select
|
NP_065970.2:p.Arg1615Lys
|
|
