Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_006019.3 | 294 | Missense Mutation | CAC,CGC | H57R | NP_006010.2 |
NM_006053.3 | 294 | Intron | NP_006044.1 | ||
XM_005273709.3 | 294 | Missense Mutation | CAC,CGC | H57R | XP_005273766.1 |
XM_011544726.2 | 294 | Missense Mutation | CAC,CGC | H57R | XP_011543028.1 |
XM_017017089.1 | 294 | Missense Mutation | CAC,CGC | H57R | XP_016872578.1 |
XM_017017090.1 | 294 | UTR 5 | XP_016872579.1 |