| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001286775.1 | 645 | Intron | NP_001273704.1 | ||
| NM_001286776.1 | 645 | Missense Mutation | CCT,TCT | P90S | NP_001273705.1 |
| NM_138779.4 | 645 | Missense Mutation | CCT,TCT | P131S | NP_620134.3 |
| XM_005254097.2 | 645 | Missense Mutation | CCT,TCT | P131S | XP_005254154.1 |
| XM_011521135.2 | 645 | Missense Mutation | CCT,TCT | P131S | XP_011519437.1 |
| XM_011521136.2 | 645 | Missense Mutation | CCT,TCT | P87S | XP_011519438.1 |
| XM_017020852.1 | 645 | Missense Mutation | CCT,TCT | P131S | XP_016876341.1 |