| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001270452.1 | 656 | Intron | NP_001257381.1 | ||
| NM_006799.3 | 656 | Missense Mutation | CCA,TCA | P186S | NP_006790.1 |
| NM_144956.2 | 656 | Missense Mutation | CCA,TCA | P184S | NP_659205.1 |
| NM_144957.2 | 656 | Missense Mutation | CCA,TCA | P186S | NP_659206.1 |
| XM_017022875.1 | 656 | Missense Mutation | CCA,TCA | P184S | XP_016878364.1 |
| XM_017022876.1 | 656 | Intron | XP_016878365.1 | ||
| XM_017022877.1 | 656 | Intron | XP_016878366.1 | ||
| XM_017022878.1 | 656 | Intron | XP_016878367.1 |