| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001009570.2 | 358 | Intron | NP_001009570.1 | ||
| NM_001166284.1 | 358 | Intron | NP_001159756.1 | ||
| NM_001166285.1 | 358 | Missense Mutation | GCC,GTC | A28V | NP_001159757.1 |
| NM_006429.3 | 358 | Missense Mutation | GCC,GTC | A72V | NP_006420.1 |
| XM_011532478.2 | 358 | Missense Mutation | GCC,GTC | A28V | XP_011530780.1 |
| XM_011532479.1 | 358 | Missense Mutation | GCC,GTC | A28V | XP_011530781.1 |