| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_007190.3 | 486 | Missense Mutation | CCT,TCT | P84S | NP_009121.1 |
| XM_005269469.2 | 486 | Missense Mutation | CCT,TCT | P84S | XP_005269526.1 |
| XM_005269470.2 | 486 | Missense Mutation | CCT,TCT | P37S | XP_005269527.1 |
| XM_017015610.1 | 486 | Missense Mutation | CCT,TCT | P37S | XP_016871099.1 |