ENST00000350026.11:c.4227T>A
|
ENSP00000055163.8:p.His1409Gln
|
|
ENST00000414678.8:c.4296T>A
|
ENSP00000412835.3:p.His1432Gln
|
|
ENST00000637015.2:c.4515T>A
|
ENSP00000489729.2:p.His1505Gln
|
|
ENST00000346085.10:c.4266T>A
|
ENSP00000344546.5:p.His1422Gln
|
|
ENST00000350026.10:c.3978T>A
|
ENSP00000055163.7:p.His1326Gln
|
|
ENST00000414678.7:c.2544T>A
|
ENSP00000412835.2:p.His848Gln
|
|
ENST00000635849.1:c.1707T>A
|
ENSP00000490948.1:p.His569Gln
|
|
ENST00000635957.1:c.1338T>A
|
ENSP00000490385.1:p.His446Gln
|
|
ENST00000636227.1:n.2849T>A
|
|
|
ENST00000636254.1:n.306T>A
|
|
|
ENST00000636930.2:c.4386T>A
MANE Select
|
ENSP00000490491.2:p.His1462Gln
|
|
ENST00000636940.1:n.2383T>A
|
|
|
ENST00000637015.1:c.1754T>A
|
|
|
ENST00000637568.1:c.1668T>A
|
|
|
ENST00000637741.1:n.1052T>A
|
|
|
ENST00000637810.1:c.1728T>A
|
ENSP00000489636.1:p.His576Gln
|
|
ENST00000637904.1:c.1887T>A
|
ENSP00000490550.1:p.His629Gln
|
|
ENST00000647938.1:c.4017T>A
|
ENSP00000498155.1:p.His1339Gln
|
|
ENST00000346085.9:c.4017T>A
|
ENSP00000344546.4:p.His1339Gln
|
|
ENST00000350026.9:c.3978T>A
|
ENSP00000055163.7:p.His1326Gln
|
|
ENST00000414678.6:c.2544T>A
|
ENSP00000412835.2:p.His848Gln
|
|
NM_017519.2:c.3978T>A
|
NP_059989.2:p.His1326Gln
|
|
NM_020732.3:c.4017T>A
|
NP_065783.3:p.His1339Gln
|
|
XM_005267069.3:c.4137T>A
|
XP_005267126.2:p.His1379Gln
|
|
XM_011535984.1:c.3216T>A
|
XP_011534286.1:p.His1072Gln
|
|
XM_011535985.1:c.3036T>A
|
XP_011534287.1:p.His1012Gln
|
|
XM_011535986.1:c.2796T>A
|
XP_011534288.1:p.His932Gln
|
|
XM_011535987.1:c.2415T>A
|
XP_011534289.1:p.His805Gln
|
|
XM_011535988.1:c.1278T>A
|
XP_011534290.1:p.His426Gln
|
|
NM_001346813.1:c.4137T>A
|
NP_001333742.1:p.His1379Gln
|
|
NM_001363725.1:c.1887T>A
|
NP_001350654.1:p.His629Gln
|
|
XM_011535984.2:c.4347T>A
|
XP_011534286.2:p.His1449Gln
|
|
XM_011535988.3:c.1278T>A
|
XP_011534290.1:p.His426Gln
|
|
XM_017011103.2:c.4248T>A
|
XP_016866592.1:p.His1416Gln
|
|
XM_017011104.1:c.4218T>A
|
XP_016866593.1:p.His1406Gln
|
|
XM_017011105.2:c.4188T>A
|
XP_016866594.1:p.His1396Gln
|
|
XM_017011106.2:c.4059T>A
|
XP_016866595.1:p.His1353Gln
|
|
XM_017011107.2:c.4038T>A
|
XP_016866596.1:p.His1346Gln
|
|
XR_002956289.1:n.4427-1891T>A
|
|
|
NM_001363725.2:c.1887T>A
|
NP_001350654.1:p.His629Gln
|
|
NM_001371656.1:c.4266T>A
|
NP_001358585.1:p.His1422Gln
|
|
NM_001374820.1:c.4266T>A
|
NP_001361749.1:p.His1422Gln
|
|
NM_001374828.1:c.4386T>A
MANE Select
|
NP_001361757.1:p.His1462Gln
|
|
NM_017519.3:c.4227T>A
|
NP_059989.3:p.His1409Gln
|
|