ENST00000215882.10:c.655A>C
MANE Select
|
ENSP00000215882.5:p.Asn219His
|
|
ENST00000215882.9:c.655A>C
|
ENSP00000215882.5:p.Asn219His
|
|
ENST00000451283.5:c.346A>C
|
ENSP00000401480.1:p.Asn116His
|
|
ENST00000461267.1:n.801A>C
|
|
|
ENST00000470922.5:n.797A>C
|
|
|
NM_001256534.1:c.676A>C
|
NP_001243463.1:p.Asn226His
|
|
NM_001287387.1:c.346A>C
|
NP_001274316.1:p.Asn116His
|
|
NM_005984.4:c.655A>C
|
NP_005975.1:p.Asn219His
|
|
NR_046298.2:n.706A>C
|
|
|
NM_005984.5:c.655A>C
MANE Select
|
NP_005975.1:p.Asn219His
|
|
NM_001256534.2:c.676A>C
|
NP_001243463.1:p.Asn226His
|
|
NM_001287387.2:c.346A>C
|
NP_001274316.1:p.Asn116His
|
|
NR_046298.3:n.579A>C
|
|
|