|
ENST00000264276.11:c.4875G>C
MANE Select
|
ENSP00000264276.6:p.Glu1625Asp
|
|
|
ENST00000439495.6:c.*1055G>C
|
ENSP00000403832.2:n.*1055G>C
|
|
|
ENST00000679409.1:c.*1580G>C
|
ENSP00000506531.1:n.*1580G>C
|
|
|
ENST00000679416.1:n.6379G>C
|
|
|
|
ENST00000679427.1:n.2546G>C
|
|
|
|
ENST00000679435.1:c.4875G>C
|
ENSP00000505218.1:p.Glu1625Asp
|
|
|
ENST00000679516.1:c.4875G>C
|
ENSP00000505187.1:p.Glu1625Asp
|
|
|
ENST00000679618.1:c.*1963G>C
|
ENSP00000506274.1:n.*1963G>C
|
|
|
ENST00000679630.1:n.6724G>C
|
|
|
|
ENST00000679635.1:n.3137G>C
|
|
|
|
ENST00000679686.1:n.4989G>C
|
|
|
|
ENST00000679701.1:n.7867G>C
|
|
|
|
ENST00000679916.1:c.*1223G>C
|
ENSP00000506172.1:n.*1223G>C
|
|
|
ENST00000680000.1:c.4875G>C
|
ENSP00000506173.1:p.Glu1625Asp
|
|
|
ENST00000680135.1:c.*2836G>C
|
ENSP00000506211.1:n.*2836G>C
|
|
|
ENST00000680149.1:c.*157G>C
|
ENSP00000506497.1:n.*157G>C
|
|
|
ENST00000680163.1:c.4875G>C
|
ENSP00000505092.1:p.Glu1625Asp
|
|
|
ENST00000680174.1:n.5566G>C
|
|
|
|
ENST00000680236.1:c.*1936G>C
|
ENSP00000506212.1:n.*1936G>C
|
|
|
ENST00000680404.1:n.390G>C
|
|
|
|
ENST00000680441.1:n.3433G>C
|
|
|
|
ENST00000680497.1:c.4977G>C
|
ENSP00000505954.1:p.Glu1659Asp
|
|
|
ENST00000680508.1:c.*31G>C
|
ENSP00000505749.1:n.*31G>C
|
|
|
ENST00000680569.1:c.*2818G>C
|
ENSP00000505522.1:n.*2818G>C
|
|
|
ENST00000680634.1:n.1383G>C
|
|
|
|
ENST00000680722.1:n.2675G>C
|
|
|
|
ENST00000680726.1:c.*157G>C
|
ENSP00000505505.1:n.*157G>C
|
|
|
ENST00000680759.1:c.4707G>C
|
ENSP00000505848.1:p.Glu1569Asp
|
|
|
ENST00000680814.1:c.4838+272G>C
|
ENSP00000505710.1:n.4838+272G>C
|
|
|
ENST00000680828.1:c.*2569G>C
|
ENSP00000505249.1:n.*2569G>C
|
|
|
ENST00000680861.1:c.4875G>C
|
ENSP00000505043.1:p.Glu1625Asp
|
|
|
ENST00000680927.1:c.*1055G>C
|
ENSP00000505473.1:n.*1055G>C
|
|
|
ENST00000680939.1:n.6816G>C
|
|
|
|
ENST00000681250.1:c.*1592G>C
|
ENSP00000505684.1:n.*1592G>C
|
|
|
ENST00000681256.1:c.*2890G>C
|
ENSP00000505446.1:n.*2890G>C
|
|
|
ENST00000681279.1:n.5741G>C
|
|
|
|
ENST00000681307.1:n.5988G>C
|
|
|
|
ENST00000681461.1:n.5643G>C
|
|
|
|
ENST00000681495.1:c.2412G>C
|
ENSP00000506085.1:p.Glu804Asp
|
|
|
ENST00000681558.1:c.2553G>C
|
ENSP00000505568.1:p.Glu851Asp
|
|
|
ENST00000681619.1:c.4872G>C
|
ENSP00000505071.1:p.Glu1624Asp
|
|
|
ENST00000681663.1:n.1781G>C
|
|
|
|
ENST00000681692.1:n.2835G>C
|
|
|
|
ENST00000681716.1:c.*2729G>C
|
ENSP00000505078.1:n.*2729G>C
|
|
|
ENST00000681768.1:c.*2539G>C
|
ENSP00000506311.1:n.*2539G>C
|
|
|
ENST00000681808.1:c.4698G>C
|
ENSP00000505219.1:p.Glu1566Asp
|
|
|
ENST00000264276.10:c.4875G>C
|
ENSP00000264276.6:p.Glu1625Asp
|
|
|
ENST00000439495.5:c.2979G>C
|
|
|
|
NM_020919.3:c.4875G>C
|
NP_065970.2:p.Glu1625Asp
|
|
|
XM_005246709.2:c.4872G>C
|
XP_005246766.1:p.Glu1624Asp
|
|
|
XM_006712654.1:c.4875G>C
|
XP_006712717.1:p.Glu1625Asp
|
|
|
XM_006712655.2:c.2811G>C
|
XP_006712718.1:p.Glu937Asp
|
|
|
XM_011511530.1:c.4536G>C
|
XP_011509832.1:p.Glu1512Asp
|
|
|
XR_922974.1:n.5153G>C
|
|
|
|
XM_006712654.3:c.4875G>C
|
XP_006712717.1:p.Glu1625Asp
|
|
|
XM_006712655.3:c.2811G>C
|
XP_006712718.1:p.Glu937Asp
|
|
|
XM_017004569.2:c.4872G>C
|
XP_016860058.1:p.Glu1624Asp
|
|
|
XM_017004572.2:c.2493G>C
|
XP_016860061.1:p.Glu831Asp
|
|
|
XM_024453024.1:c.4536G>C
|
XP_024308792.1:p.Glu1512Asp
|
|
|
XM_024453025.1:c.2808G>C
|
XP_024308793.1:p.Glu936Asp
|
|
|
XR_001738864.2:n.4990G>C
|
|
|
|
XR_001738865.2:n.4987G>C
|
|
|
|
XR_001738866.2:n.5153G>C
|
|
|
|
XR_001738867.2:n.5150G>C
|
|
|
|
XR_002959320.1:n.4046G>C
|
|
|
|
NM_020919.4:c.4875G>C
MANE Select
|
NP_065970.2:p.Glu1625Asp
|
|
