| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001282715.1 | 408 | Intron | NP_001269644.1 | ||
| NM_182487.3 | 408 | Missense Mutation | CCC,TCC | P99S | NP_872293.2 |
| XM_005251760.4 | 408 | Missense Mutation | CCC,TCC | P99S | XP_005251817.1 |
| XM_006716989.2 | 408 | Missense Mutation | CCC,TCC | P99S | XP_006717052.1 |