ENST00000215882.10:c.712A>C
MANE Select
|
ENSP00000215882.5:p.Asn238His
|
|
ENST00000215882.9:c.712A>C
|
ENSP00000215882.5:p.Asn238His
|
|
ENST00000451283.5:c.403A>C
|
ENSP00000401480.1:p.Asn135His
|
|
ENST00000470922.5:n.854A>C
|
|
|
NM_001256534.1:c.733A>C
|
NP_001243463.1:p.Asn245His
|
|
NM_001287387.1:c.403A>C
|
NP_001274316.1:p.Asn135His
|
|
NM_005984.4:c.712A>C
|
NP_005975.1:p.Asn238His
|
|
NR_046298.2:n.763A>C
|
|
|
NM_005984.5:c.712A>C
MANE Select
|
NP_005975.1:p.Asn238His
|
|
NM_001256534.2:c.733A>C
|
NP_001243463.1:p.Asn245His
|
|
NM_001287387.2:c.403A>C
|
NP_001274316.1:p.Asn135His
|
|
NR_046298.3:n.636A>C
|
|
|