Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001177388.1 | 279 | Missense Mutation | CAT,CCT | H64P | NP_001170859.1 |
NM_002306.3 | 279 | Missense Mutation | CAT,CCT | H64P | NP_002297.2 |
XM_011536759.2 | 279 | Missense Mutation | CAT,CCT | H78P | XP_011535061.2 |