| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001163075.1 | 145 | Missense Mutation | CCT,TCT | P27S | NP_001156547.1 |
| XM_011524152.2 | 145 | Missense Mutation | CCT,TCT | P31S | XP_011522454.1 |
| XM_017023997.1 | 145 | Missense Mutation | CCT,TCT | P31S | XP_016879486.1 |
| XM_017023998.1 | 145 | Missense Mutation | CCT,TCT | P27S | XP_016879487.1 |
| XM_017023999.1 | 145 | Intron | XP_016879488.1 | ||
| XM_017024000.1 | 145 | UTR 5 | XP_016879489.1 | ||
| XM_017024001.1 | 145 | UTR 5 | XP_016879490.1 |