ENST00000350026.11:c.4733A=
|
ENSP00000055163.8:p.His1578=
|
|
ENST00000414678.8:c.4802A=
|
ENSP00000412835.3:p.His1601=
|
|
ENST00000637015.2:c.5021A=
|
ENSP00000489729.2:p.His1674=
|
|
ENST00000346085.10:c.4772A=
|
ENSP00000344546.5:p.His1591=
|
|
ENST00000350026.10:c.4484A=
|
ENSP00000055163.7:p.His1495=
|
|
ENST00000414678.7:c.3050A=
|
ENSP00000412835.2:p.His1017=
|
|
ENST00000635849.1:c.2213A=
|
ENSP00000490948.1:p.His738=
|
|
ENST00000635957.1:c.1844A=
|
ENSP00000490385.1:p.His615=
|
|
ENST00000636227.1:n.3355A=
|
|
|
ENST00000636254.1:n.812A=
|
|
|
ENST00000636930.2:c.4892A=
MANE Select
|
ENSP00000490491.2:p.His1631=
|
|
ENST00000636940.1:n.2889A=
|
|
|
ENST00000637015.1:c.2260A=
|
|
|
ENST00000637568.1:c.2174A=
|
|
|
ENST00000637741.1:n.1558A=
|
|
|
ENST00000637810.1:c.2234A=
|
ENSP00000489636.1:p.His745=
|
|
ENST00000637904.1:c.2393A=
|
ENSP00000490550.1:p.His798=
|
|
ENST00000647938.1:c.4523A=
|
ENSP00000498155.1:p.His1508=
|
|
ENST00000346085.9:c.4523A=
|
ENSP00000344546.4:p.His1508=
|
|
ENST00000350026.9:c.4484A=
|
ENSP00000055163.7:p.His1495=
|
|
ENST00000414678.6:c.3050A=
|
ENSP00000412835.2:p.His1017=
|
|
NM_017519.2:c.4484A=
|
NP_059989.2:p.His1495=
|
|
NM_020732.3:c.4523A=
|
NP_065783.3:p.His1508=
|
|
XM_005267069.3:c.4643A=
|
XP_005267126.2:p.His1548=
|
|
XM_011535984.1:c.3722A=
|
XP_011534286.1:p.His1241=
|
|
XM_011535985.1:c.3542A=
|
XP_011534287.1:p.His1181=
|
|
XM_011535986.1:c.3302A=
|
XP_011534288.1:p.His1101=
|
|
XM_011535987.1:c.2921A=
|
XP_011534289.1:p.His974=
|
|
XM_011535988.1:c.1784A=
|
XP_011534290.1:p.His595=
|
|
NM_001346813.1:c.4643A=
|
NP_001333742.1:p.His1548=
|
|
NM_001363725.1:c.2393A=
|
NP_001350654.1:p.His798=
|
|
XM_011535984.2:c.4853A=
|
XP_011534286.2:p.His1618=
|
|
XM_011535988.3:c.1784A=
|
XP_011534290.1:p.His595=
|
|
XM_017011103.2:c.4754A=
|
XP_016866592.1:p.His1585=
|
|
XM_017011104.1:c.4724A=
|
XP_016866593.1:p.His1575=
|
|
XM_017011105.2:c.4694A=
|
XP_016866594.1:p.His1565=
|
|
XM_017011106.2:c.4565A=
|
XP_016866595.1:p.His1522=
|
|
XM_017011107.2:c.4544A=
|
XP_016866596.1:p.His1515=
|
|
XR_002956289.1:n.4839A=
|
|
|
NM_001363725.2:c.2393A=
|
NP_001350654.1:p.His798=
|
|
NM_001371656.1:c.4772A=
|
NP_001358585.1:p.His1591=
|
|
NM_001374820.1:c.4772A=
|
NP_001361749.1:p.His1591=
|
|
NM_001374828.1:c.4892A=
MANE Select
|
NP_001361757.1:p.His1631=
|
|
NM_017519.3:c.4733A=
|
NP_059989.3:p.His1578=
|
|