ENST00000350026.11:c.3868C>A
|
ENSP00000055163.8:p.His1290Asn
|
|
ENST00000414678.8:c.3937C>A
|
ENSP00000412835.3:p.His1313Asn
|
|
ENST00000637015.2:c.4156C>A
|
ENSP00000489729.2:p.His1386Asn
|
|
ENST00000346085.10:c.3907C>A
|
ENSP00000344546.5:p.His1303Asn
|
|
ENST00000350026.10:c.3619C>A
|
ENSP00000055163.7:p.His1207Asn
|
|
ENST00000414678.7:c.2185C>A
|
ENSP00000412835.2:p.His729Asn
|
|
ENST00000635849.1:c.1348C>A
|
ENSP00000490948.1:p.His450Asn
|
|
ENST00000635957.1:c.982C>A
|
ENSP00000490385.1:p.His328Asn
|
|
ENST00000636930.2:c.4027C>A
MANE Select
|
ENSP00000490491.2:p.His1343Asn
|
|
ENST00000636940.1:n.2024C>A
|
|
|
ENST00000637015.1:c.1395C>A
|
|
|
ENST00000637568.1:c.1309C>A
|
|
|
ENST00000637741.1:n.693C>A
|
|
|
ENST00000637810.1:c.1369C>A
|
ENSP00000489636.1:p.His457Asn
|
|
ENST00000637904.1:c.1528C>A
|
ENSP00000490550.1:p.His510Asn
|
|
ENST00000647938.1:c.3658C>A
|
ENSP00000498155.1:p.His1220Asn
|
|
ENST00000346085.9:c.3658C>A
|
ENSP00000344546.4:p.His1220Asn
|
|
ENST00000350026.9:c.3619C>A
|
ENSP00000055163.7:p.His1207Asn
|
|
ENST00000414678.6:c.2185C>A
|
ENSP00000412835.2:p.His729Asn
|
|
NM_017519.2:c.3619C>A
|
NP_059989.2:p.His1207Asn
|
|
NM_020732.3:c.3658C>A
|
NP_065783.3:p.His1220Asn
|
|
XM_005267069.3:c.3778C>A
|
XP_005267126.2:p.His1260Asn
|
|
XM_011535984.1:c.2857C>A
|
XP_011534286.1:p.His953Asn
|
|
XM_011535985.1:c.2677C>A
|
XP_011534287.1:p.His893Asn
|
|
XM_011535986.1:c.2437C>A
|
XP_011534288.1:p.His813Asn
|
|
XM_011535987.1:c.2056C>A
|
XP_011534289.1:p.His686Asn
|
|
XM_011535988.1:c.919C>A
|
XP_011534290.1:p.His307Asn
|
|
NM_001346813.1:c.3778C>A
|
NP_001333742.1:p.His1260Asn
|
|
NM_001363725.1:c.1528C>A
|
NP_001350654.1:p.His510Asn
|
|
XM_011535984.2:c.3988C>A
|
XP_011534286.2:p.His1330Asn
|
|
XM_011535988.3:c.919C>A
|
XP_011534290.1:p.His307Asn
|
|
XM_017011103.2:c.3889C>A
|
XP_016866592.1:p.His1297Asn
|
|
XM_017011104.1:c.3859C>A
|
XP_016866593.1:p.His1287Asn
|
|
XM_017011105.2:c.3829C>A
|
XP_016866594.1:p.His1277Asn
|
|
XM_017011106.2:c.3700C>A
|
XP_016866595.1:p.His1234Asn
|
|
XM_017011107.2:c.3679C>A
|
XP_016866596.1:p.His1227Asn
|
|
XR_002956289.1:n.4071C>A
|
|
|
NM_001363725.2:c.1528C>A
|
NP_001350654.1:p.His510Asn
|
|
NM_001371656.1:c.3907C>A
|
NP_001358585.1:p.His1303Asn
|
|
NM_001374820.1:c.3907C>A
|
NP_001361749.1:p.His1303Asn
|
|
NM_001374828.1:c.4027C>A
MANE Select
|
NP_001361757.1:p.His1343Asn
|
|
NM_017519.3:c.3868C>A
|
NP_059989.3:p.His1290Asn
|
|