Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_052853.3 | 696 | Missense Mutation | CAC,CGC | H98R | NP_443085.2 |
XM_006716170.3 | 696 | Missense Mutation | CAC,CGC | H98R | XP_006716233.1 |
XM_011516675.2 | 696 | Missense Mutation | CAC,CGC | H98R | XP_011514977.1 |