ENST00000350026.11:c.4293C>G
|
ENSP00000055163.8:p.His1431Gln
|
|
ENST00000414678.8:c.4362C>G
|
ENSP00000412835.3:p.His1454Gln
|
|
ENST00000637015.2:c.4581C>G
|
ENSP00000489729.2:p.His1527Gln
|
|
ENST00000346085.10:c.4332C>G
|
ENSP00000344546.5:p.His1444Gln
|
|
ENST00000350026.10:c.4044C>G
|
ENSP00000055163.7:p.His1348Gln
|
|
ENST00000414678.7:c.2610C>G
|
ENSP00000412835.2:p.His870Gln
|
|
ENST00000635849.1:c.1773C>G
|
ENSP00000490948.1:p.His591Gln
|
|
ENST00000635957.1:c.1404C>G
|
ENSP00000490385.1:p.His468Gln
|
|
ENST00000636227.1:n.2915C>G
|
|
|
ENST00000636254.1:n.372C>G
|
|
|
ENST00000636930.2:c.4452C>G
MANE Select
|
ENSP00000490491.2:p.His1484Gln
|
|
ENST00000636940.1:n.2449C>G
|
|
|
ENST00000637015.1:c.1820C>G
|
|
|
ENST00000637568.1:c.1734C>G
|
|
|
ENST00000637741.1:n.1118C>G
|
|
|
ENST00000637810.1:c.1794C>G
|
ENSP00000489636.1:p.His598Gln
|
|
ENST00000637904.1:c.1953C>G
|
ENSP00000490550.1:p.His651Gln
|
|
ENST00000647938.1:c.4083C>G
|
ENSP00000498155.1:p.His1361Gln
|
|
ENST00000346085.9:c.4083C>G
|
ENSP00000344546.4:p.His1361Gln
|
|
ENST00000350026.9:c.4044C>G
|
ENSP00000055163.7:p.His1348Gln
|
|
ENST00000414678.6:c.2610C>G
|
ENSP00000412835.2:p.His870Gln
|
|
NM_017519.2:c.4044C>G
|
NP_059989.2:p.His1348Gln
|
|
NM_020732.3:c.4083C>G
|
NP_065783.3:p.His1361Gln
|
|
XM_005267069.3:c.4203C>G
|
XP_005267126.2:p.His1401Gln
|
|
XM_011535984.1:c.3282C>G
|
XP_011534286.1:p.His1094Gln
|
|
XM_011535985.1:c.3102C>G
|
XP_011534287.1:p.His1034Gln
|
|
XM_011535986.1:c.2862C>G
|
XP_011534288.1:p.His954Gln
|
|
XM_011535987.1:c.2481C>G
|
XP_011534289.1:p.His827Gln
|
|
XM_011535988.1:c.1344C>G
|
XP_011534290.1:p.His448Gln
|
|
NM_001346813.1:c.4203C>G
|
NP_001333742.1:p.His1401Gln
|
|
NM_001363725.1:c.1953C>G
|
NP_001350654.1:p.His651Gln
|
|
XM_011535984.2:c.4413C>G
|
XP_011534286.2:p.His1471Gln
|
|
XM_011535988.3:c.1344C>G
|
XP_011534290.1:p.His448Gln
|
|
XM_017011103.2:c.4314C>G
|
XP_016866592.1:p.His1438Gln
|
|
XM_017011104.1:c.4284C>G
|
XP_016866593.1:p.His1428Gln
|
|
XM_017011105.2:c.4254C>G
|
XP_016866594.1:p.His1418Gln
|
|
XM_017011106.2:c.4125C>G
|
XP_016866595.1:p.His1375Gln
|
|
XM_017011107.2:c.4104C>G
|
XP_016866596.1:p.His1368Gln
|
|
XR_002956289.1:n.4427-1825C>G
|
|
|
NM_001363725.2:c.1953C>G
|
NP_001350654.1:p.His651Gln
|
|
NM_001371656.1:c.4332C>G
|
NP_001358585.1:p.His1444Gln
|
|
NM_001374820.1:c.4332C>G
|
NP_001361749.1:p.His1444Gln
|
|
NM_001374828.1:c.4452C>G
MANE Select
|
NP_001361757.1:p.His1484Gln
|
|
NM_017519.3:c.4293C>G
|
NP_059989.3:p.His1431Gln
|
|