| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_152512.3 | 1599 | Silent Mutation | CCA,CCG | P439P | NP_689725.2 |
| XM_006724149.3 | 1599 | Silent Mutation | CCA,CCG | P439P | XP_006724212.1 |
| XM_006724150.3 | 1599 | Silent Mutation | CCA,CCG | P386P | XP_006724213.1 |
| XM_006724151.1 | 1599 | Silent Mutation | CCA,CCG | P326P | XP_006724214.1 |
| XM_006724153.3 | 1599 | Intron | XP_006724216.1 | ||
| XM_011529927.2 | 1599 | Silent Mutation | CCA,CCG | P418P | XP_011528229.1 |
| XM_011529928.2 | 1599 | Silent Mutation | CCA,CCG | P358P | XP_011528230.1 |
| XM_011529930.2 | 1599 | Silent Mutation | CCA,CCG | P175P | XP_011528232.1 |
| XM_011529931.2 | 1599 | Intron | XP_011528233.1 |