| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001146094.1 | 410 | Missense Mutation | CCT,TCT | P39S | NP_001139566.1 |
| NM_001146095.1 | 410 | Missense Mutation | CCT,TCT | P39S | NP_001139567.1 |
| NM_001146096.1 | 410 | Missense Mutation | CCT,TCT | P39S | NP_001139568.1 |
| NM_014967.4 | 410 | Missense Mutation | CCT,TCT | P39S | NP_055782.3 |
| XM_005254232.4 | 410 | Missense Mutation | CCT,TCT | P39S | XP_005254289.1 |
| XM_005254234.4 | 410 | Missense Mutation | CCT,TCT | P39S | XP_005254291.1 |
| XM_005254235.3 | 410 | Missense Mutation | CCT,TCT | P39S | XP_005254292.1 |
| XM_011521370.2 | 410 | Intron | XP_011519672.1 | ||
| XM_011521371.1 | 410 | UTR 5 | XP_011519673.1 | ||
| XM_011521372.2 | 410 | Missense Mutation | CCT,TCT | P39S | XP_011519674.1 |
| XM_017022012.1 | 410 | UTR 5 | XP_016877501.1 | ||
| XM_017022013.1 | 410 | UTR 5 | XP_016877502.1 |