Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001195286.1 | 389 | Missense Mutation | CAG,CCG | Q88P | NP_001182215.1 |
NM_002460.3 | 389 | Missense Mutation | CAG,CCG | Q88P | NP_002451.2 |
XM_006715090.2 | 389 | Missense Mutation | CAG,CCG | Q88P | XP_006715153.1 |