ENST00000350026.11:c.4533C>G
|
ENSP00000055163.8:p.His1511Gln
|
|
ENST00000414678.8:c.4602C>G
|
ENSP00000412835.3:p.His1534Gln
|
|
ENST00000637015.2:c.4821C>G
|
ENSP00000489729.2:p.His1607Gln
|
|
ENST00000346085.10:c.4572C>G
|
ENSP00000344546.5:p.His1524Gln
|
|
ENST00000350026.10:c.4284C>G
|
ENSP00000055163.7:p.His1428Gln
|
|
ENST00000414678.7:c.2850C>G
|
ENSP00000412835.2:p.His950Gln
|
|
ENST00000635849.1:c.2013C>G
|
ENSP00000490948.1:p.His671Gln
|
|
ENST00000635957.1:c.1644C>G
|
ENSP00000490385.1:p.His548Gln
|
|
ENST00000636227.1:n.3155C>G
|
|
|
ENST00000636254.1:n.612C>G
|
|
|
ENST00000636930.2:c.4692C>G
MANE Select
|
ENSP00000490491.2:p.His1564Gln
|
|
ENST00000636940.1:n.2689C>G
|
|
|
ENST00000637015.1:c.2060C>G
|
|
|
ENST00000637568.1:c.1974C>G
|
|
|
ENST00000637741.1:n.1358C>G
|
|
|
ENST00000637810.1:c.2034C>G
|
ENSP00000489636.1:p.His678Gln
|
|
ENST00000637904.1:c.2193C>G
|
ENSP00000490550.1:p.His731Gln
|
|
ENST00000647938.1:c.4323C>G
|
ENSP00000498155.1:p.His1441Gln
|
|
ENST00000346085.9:c.4323C>G
|
ENSP00000344546.4:p.His1441Gln
|
|
ENST00000350026.9:c.4284C>G
|
ENSP00000055163.7:p.His1428Gln
|
|
ENST00000414678.6:c.2850C>G
|
ENSP00000412835.2:p.His950Gln
|
|
NM_017519.2:c.4284C>G
|
NP_059989.2:p.His1428Gln
|
|
NM_020732.3:c.4323C>G
|
NP_065783.3:p.His1441Gln
|
|
XM_005267069.3:c.4443C>G
|
XP_005267126.2:p.His1481Gln
|
|
XM_011535984.1:c.3522C>G
|
XP_011534286.1:p.His1174Gln
|
|
XM_011535985.1:c.3342C>G
|
XP_011534287.1:p.His1114Gln
|
|
XM_011535986.1:c.3102C>G
|
XP_011534288.1:p.His1034Gln
|
|
XM_011535987.1:c.2721C>G
|
XP_011534289.1:p.His907Gln
|
|
XM_011535988.1:c.1584C>G
|
XP_011534290.1:p.His528Gln
|
|
NM_001346813.1:c.4443C>G
|
NP_001333742.1:p.His1481Gln
|
|
NM_001363725.1:c.2193C>G
|
NP_001350654.1:p.His731Gln
|
|
XM_011535984.2:c.4653C>G
|
XP_011534286.2:p.His1551Gln
|
|
XM_011535988.3:c.1584C>G
|
XP_011534290.1:p.His528Gln
|
|
XM_017011103.2:c.4554C>G
|
XP_016866592.1:p.His1518Gln
|
|
XM_017011104.1:c.4524C>G
|
XP_016866593.1:p.His1508Gln
|
|
XM_017011105.2:c.4494C>G
|
XP_016866594.1:p.His1498Gln
|
|
XM_017011106.2:c.4365C>G
|
XP_016866595.1:p.His1455Gln
|
|
XM_017011107.2:c.4344C>G
|
XP_016866596.1:p.His1448Gln
|
|
XR_002956289.1:n.4639C>G
|
|
|
NM_001363725.2:c.2193C>G
|
NP_001350654.1:p.His731Gln
|
|
NM_001371656.1:c.4572C>G
|
NP_001358585.1:p.His1524Gln
|
|
NM_001374820.1:c.4572C>G
|
NP_001361749.1:p.His1524Gln
|
|
NM_001374828.1:c.4692C>G
MANE Select
|
NP_001361757.1:p.His1564Gln
|
|
NM_017519.3:c.4533C>G
|
NP_059989.3:p.His1511Gln
|
|