ENST00000350026.11:c.4296G>T
|
ENSP00000055163.8:p.Gln1432His
|
|
ENST00000414678.8:c.4365G>T
|
ENSP00000412835.3:p.Gln1455His
|
|
ENST00000637015.2:c.4584G>T
|
ENSP00000489729.2:p.Gln1528His
|
|
ENST00000346085.10:c.4335G>T
|
ENSP00000344546.5:p.Gln1445His
|
|
ENST00000350026.10:c.4047G>T
|
ENSP00000055163.7:p.Gln1349His
|
|
ENST00000414678.7:c.2613G>T
|
ENSP00000412835.2:p.Gln871His
|
|
ENST00000635849.1:c.1776G>T
|
ENSP00000490948.1:p.Gln592His
|
|
ENST00000635957.1:c.1407G>T
|
ENSP00000490385.1:p.Gln469His
|
|
ENST00000636227.1:n.2918G>T
|
|
|
ENST00000636254.1:n.375G>T
|
|
|
ENST00000636930.2:c.4455G>T
MANE Select
|
ENSP00000490491.2:p.Gln1485His
|
|
ENST00000636940.1:n.2452G>T
|
|
|
ENST00000637015.1:c.1823G>T
|
|
|
ENST00000637568.1:c.1737G>T
|
|
|
ENST00000637741.1:n.1121G>T
|
|
|
ENST00000637810.1:c.1797G>T
|
ENSP00000489636.1:p.Gln599His
|
|
ENST00000637904.1:c.1956G>T
|
ENSP00000490550.1:p.Gln652His
|
|
ENST00000647938.1:c.4086G>T
|
ENSP00000498155.1:p.Gln1362His
|
|
ENST00000346085.9:c.4086G>T
|
ENSP00000344546.4:p.Gln1362His
|
|
ENST00000350026.9:c.4047G>T
|
ENSP00000055163.7:p.Gln1349His
|
|
ENST00000414678.6:c.2613G>T
|
ENSP00000412835.2:p.Gln871His
|
|
NM_017519.2:c.4047G>T
|
NP_059989.2:p.Gln1349His
|
|
NM_020732.3:c.4086G>T
|
NP_065783.3:p.Gln1362His
|
|
XM_005267069.3:c.4206G>T
|
XP_005267126.2:p.Gln1402His
|
|
XM_011535984.1:c.3285G>T
|
XP_011534286.1:p.Gln1095His
|
|
XM_011535985.1:c.3105G>T
|
XP_011534287.1:p.Gln1035His
|
|
XM_011535986.1:c.2865G>T
|
XP_011534288.1:p.Gln955His
|
|
XM_011535987.1:c.2484G>T
|
XP_011534289.1:p.Gln828His
|
|
XM_011535988.1:c.1347G>T
|
XP_011534290.1:p.Gln449His
|
|
NM_001346813.1:c.4206G>T
|
NP_001333742.1:p.Gln1402His
|
|
NM_001363725.1:c.1956G>T
|
NP_001350654.1:p.Gln652His
|
|
XM_011535984.2:c.4416G>T
|
XP_011534286.2:p.Gln1472His
|
|
XM_011535988.3:c.1347G>T
|
XP_011534290.1:p.Gln449His
|
|
XM_017011103.2:c.4317G>T
|
XP_016866592.1:p.Gln1439His
|
|
XM_017011104.1:c.4287G>T
|
XP_016866593.1:p.Gln1429His
|
|
XM_017011105.2:c.4257G>T
|
XP_016866594.1:p.Gln1419His
|
|
XM_017011106.2:c.4128G>T
|
XP_016866595.1:p.Gln1376His
|
|
XM_017011107.2:c.4107G>T
|
XP_016866596.1:p.Gln1369His
|
|
XR_002956289.1:n.4427-1822G>T
|
|
|
NM_001363725.2:c.1956G>T
|
NP_001350654.1:p.Gln652His
|
|
NM_001371656.1:c.4335G>T
|
NP_001358585.1:p.Gln1445His
|
|
NM_001374820.1:c.4335G>T
|
NP_001361749.1:p.Gln1445His
|
|
NM_001374828.1:c.4455G>T
MANE Select
|
NP_001361757.1:p.Gln1485His
|
|
NM_017519.3:c.4296G>T
|
NP_059989.3:p.Gln1432His
|
|