| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001164372.1 | 352 | Silent Mutation | TCC,TCG | S51S | NP_001157844.1 |
| NM_001164373.1 | 352 | Intron | NP_001157845.1 | ||
| NM_016301.3 | 352 | Intron | NP_057385.3 | ||
| XM_005253896.4 | 352 | Missense Mutation | CCG,CGG | P112R | XP_005253953.3 |
| XM_017019394.1 | 352 | Intron | XP_016874883.1 |