ENST00000350026.11:c.4743G>T
|
ENSP00000055163.8:p.Gln1581His
|
|
ENST00000414678.8:c.4812G>T
|
ENSP00000412835.3:p.Gln1604His
|
|
ENST00000637015.2:c.5031G>T
|
ENSP00000489729.2:p.Gln1677His
|
|
ENST00000346085.10:c.4782G>T
|
ENSP00000344546.5:p.Gln1594His
|
|
ENST00000350026.10:c.4494G>T
|
ENSP00000055163.7:p.Gln1498His
|
|
ENST00000414678.7:c.3060G>T
|
ENSP00000412835.2:p.Gln1020His
|
|
ENST00000635849.1:c.2223G>T
|
ENSP00000490948.1:p.Gln741His
|
|
ENST00000635957.1:c.1854G>T
|
ENSP00000490385.1:p.Gln618His
|
|
ENST00000636227.1:n.3365G>T
|
|
|
ENST00000636254.1:n.822G>T
|
|
|
ENST00000636930.2:c.4902G>T
MANE Select
|
ENSP00000490491.2:p.Gln1634His
|
|
ENST00000636940.1:n.2899G>T
|
|
|
ENST00000637015.1:c.2270G>T
|
|
|
ENST00000637568.1:c.2184G>T
|
|
|
ENST00000637741.1:n.1568G>T
|
|
|
ENST00000637810.1:c.2244G>T
|
ENSP00000489636.1:p.Gln748His
|
|
ENST00000637904.1:c.2403G>T
|
ENSP00000490550.1:p.Gln801His
|
|
ENST00000647938.1:c.4533G>T
|
ENSP00000498155.1:p.Gln1511His
|
|
ENST00000346085.9:c.4533G>T
|
ENSP00000344546.4:p.Gln1511His
|
|
ENST00000350026.9:c.4494G>T
|
ENSP00000055163.7:p.Gln1498His
|
|
ENST00000414678.6:c.3060G>T
|
ENSP00000412835.2:p.Gln1020His
|
|
NM_017519.2:c.4494G>T
|
NP_059989.2:p.Gln1498His
|
|
NM_020732.3:c.4533G>T
|
NP_065783.3:p.Gln1511His
|
|
XM_005267069.3:c.4653G>T
|
XP_005267126.2:p.Gln1551His
|
|
XM_011535984.1:c.3732G>T
|
XP_011534286.1:p.Gln1244His
|
|
XM_011535985.1:c.3552G>T
|
XP_011534287.1:p.Gln1184His
|
|
XM_011535986.1:c.3312G>T
|
XP_011534288.1:p.Gln1104His
|
|
XM_011535987.1:c.2931G>T
|
XP_011534289.1:p.Gln977His
|
|
XM_011535988.1:c.1794G>T
|
XP_011534290.1:p.Gln598His
|
|
NM_001346813.1:c.4653G>T
|
NP_001333742.1:p.Gln1551His
|
|
NM_001363725.1:c.2403G>T
|
NP_001350654.1:p.Gln801His
|
|
XM_011535984.2:c.4863G>T
|
XP_011534286.2:p.Gln1621His
|
|
XM_011535988.3:c.1794G>T
|
XP_011534290.1:p.Gln598His
|
|
XM_017011103.2:c.4764G>T
|
XP_016866592.1:p.Gln1588His
|
|
XM_017011104.1:c.4734G>T
|
XP_016866593.1:p.Gln1578His
|
|
XM_017011105.2:c.4704G>T
|
XP_016866594.1:p.Gln1568His
|
|
XM_017011106.2:c.4575G>T
|
XP_016866595.1:p.Gln1525His
|
|
XM_017011107.2:c.4554G>T
|
XP_016866596.1:p.Gln1518His
|
|
XR_002956289.1:n.4849G>T
|
|
|
NM_001363725.2:c.2403G>T
|
NP_001350654.1:p.Gln801His
|
|
NM_001371656.1:c.4782G>T
|
NP_001358585.1:p.Gln1594His
|
|
NM_001374820.1:c.4782G>T
|
NP_001361749.1:p.Gln1594His
|
|
NM_001374828.1:c.4902G>T
MANE Select
|
NP_001361757.1:p.Gln1634His
|
|
NM_017519.3:c.4743G>T
|
NP_059989.3:p.Gln1581His
|
|