Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_178536.3 | 478 | Missense Mutation | CCG,CTG | P97L | NP_848631.2 |
XM_006717065.3 | 478 | Missense Mutation | CCG,CTG | P97L | XP_006717128.1 |
XM_011518560.2 | 478 | Missense Mutation | CCG,CTG | P124L | XP_011516862.1 |
XM_011518561.2 | 478 | Missense Mutation | CCG,CTG | P125L | XP_011516863.2 |
XM_011518562.2 | 478 | Missense Mutation | CCG,CTG | P97L | XP_011516864.1 |
XM_017014631.1 | 478 | Missense Mutation | CCG,CTG | P125L | XP_016870120.1 |
XM_017014632.1 | 478 | Missense Mutation | CCG,CTG | P125L | XP_016870121.1 |