ENST00000699947.1:c.484A>C
|
ENSP00000514703.1:p.Asn162His
|
|
ENST00000699948.1:c.484A>C
|
ENSP00000514704.1:p.Asn162His
|
|
ENST00000699950.1:n.436A>C
|
|
|
ENST00000382745.9:c.484A>C
MANE Select
|
ENSP00000372193.4:p.Asn162His
|
|
ENST00000262318.12:c.412A>C
|
ENSP00000262318.8:p.Asn138His
|
|
ENST00000382745.8:c.484A>C
|
ENSP00000372193.4:p.Asn162His
|
|
ENST00000448525.5:c.412A>C
|
ENSP00000410907.1:p.Asn138His
|
|
ENST00000561665.5:n.514A>C
|
|
|
ENST00000567139.1:n.535A>C
|
|
|
ENST00000569851.6:c.310A>C
|
ENSP00000461009.1:p.Asn104His
|
|
NM_001114331.2:c.412A>C
|
NP_001107803.1:p.Asn138His
|
|
NM_001287.5:c.484A>C
|
NP_001278.1:p.Asn162His
|
|
XM_011522354.1:c.310A>C
|
XP_011520656.1:p.Asn104His
|
|
NM_001287.6:c.484A>C
MANE Select
|
NP_001278.1:p.Asn162His
|
|
NM_001114331.3:c.412A>C
|
NP_001107803.1:p.Asn138His
|
|