| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001270.2 | 2998 | Missense Mutation | CCT,TCT | P1684S | NP_001261.2 |
| XM_005271866.4 | 2998 | Missense Mutation | CCT,TCT | P1772S | XP_005271923.1 |
| XM_005271867.4 | 2998 | Missense Mutation | CCT,TCT | P1684S | XP_005271924.1 |
| XM_011543112.2 | 2998 | UTR 3 | XP_011541414.1 | ||
| XM_017008991.1 | 2998 | Missense Mutation | CCT,TCT | P843S | XP_016864480.1 |
| XM_017008992.1 | 2998 | Missense Mutation | CCT,TCT | P843S | XP_016864481.1 |