ENST00000350026.11:c.3964A>C
|
ENSP00000055163.8:p.Asn1322His
|
|
ENST00000414678.8:c.4033A>C
|
ENSP00000412835.3:p.Asn1345His
|
|
ENST00000637015.2:c.4252A>C
|
ENSP00000489729.2:p.Asn1418His
|
|
ENST00000346085.10:c.4003A>C
|
ENSP00000344546.5:p.Asn1335His
|
|
ENST00000350026.10:c.3715A>C
|
ENSP00000055163.7:p.Asn1239His
|
|
ENST00000414678.7:c.2281A>C
|
ENSP00000412835.2:p.Asn761His
|
|
ENST00000635849.1:c.1444A>C
|
ENSP00000490948.1:p.Asn482His
|
|
ENST00000635957.1:c.1075A>C
|
ENSP00000490385.1:p.Asn359His
|
|
ENST00000636930.2:c.4123A>C
MANE Select
|
ENSP00000490491.2:p.Asn1375His
|
|
ENST00000636940.1:n.2120A>C
|
|
|
ENST00000637015.1:c.1491A>C
|
|
|
ENST00000637568.1:c.1405A>C
|
|
|
ENST00000637741.1:n.789A>C
|
|
|
ENST00000637810.1:c.1465A>C
|
ENSP00000489636.1:p.Asn489His
|
|
ENST00000637904.1:c.1624A>C
|
ENSP00000490550.1:p.Asn542His
|
|
ENST00000647938.1:c.3754A>C
|
ENSP00000498155.1:p.Asn1252His
|
|
ENST00000346085.9:c.3754A>C
|
ENSP00000344546.4:p.Asn1252His
|
|
ENST00000350026.9:c.3715A>C
|
ENSP00000055163.7:p.Asn1239His
|
|
ENST00000414678.6:c.2281A>C
|
ENSP00000412835.2:p.Asn761His
|
|
NM_017519.2:c.3715A>C
|
NP_059989.2:p.Asn1239His
|
|
NM_020732.3:c.3754A>C
|
NP_065783.3:p.Asn1252His
|
|
XM_005267069.3:c.3874A>C
|
XP_005267126.2:p.Asn1292His
|
|
XM_011535984.1:c.2953A>C
|
XP_011534286.1:p.Asn985His
|
|
XM_011535985.1:c.2773A>C
|
XP_011534287.1:p.Asn925His
|
|
XM_011535986.1:c.2533A>C
|
XP_011534288.1:p.Asn845His
|
|
XM_011535987.1:c.2152A>C
|
XP_011534289.1:p.Asn718His
|
|
XM_011535988.1:c.1015A>C
|
XP_011534290.1:p.Asn339His
|
|
NM_001346813.1:c.3874A>C
|
NP_001333742.1:p.Asn1292His
|
|
NM_001363725.1:c.1624A>C
|
NP_001350654.1:p.Asn542His
|
|
XM_011535984.2:c.4084A>C
|
XP_011534286.2:p.Asn1362His
|
|
XM_011535988.3:c.1015A>C
|
XP_011534290.1:p.Asn339His
|
|
XM_017011103.2:c.3985A>C
|
XP_016866592.1:p.Asn1329His
|
|
XM_017011104.1:c.3955A>C
|
XP_016866593.1:p.Asn1319His
|
|
XM_017011105.2:c.3925A>C
|
XP_016866594.1:p.Asn1309His
|
|
XM_017011106.2:c.3796A>C
|
XP_016866595.1:p.Asn1266His
|
|
XM_017011107.2:c.3775A>C
|
XP_016866596.1:p.Asn1259His
|
|
XR_002956289.1:n.4167A>C
|
|
|
NM_001363725.2:c.1624A>C
|
NP_001350654.1:p.Asn542His
|
|
NM_001371656.1:c.4003A>C
|
NP_001358585.1:p.Asn1335His
|
|
NM_001374820.1:c.4003A>C
|
NP_001361749.1:p.Asn1335His
|
|
NM_001374828.1:c.4123A>C
MANE Select
|
NP_001361757.1:p.Asn1375His
|
|
NM_017519.3:c.3964A>C
|
NP_059989.3:p.Asn1322His
|
|