| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_020956.2 | 5284 | UTR 3 | NP_066007.1 | ||
| NM_181882.2 | 5284 | Missense Mutation | CCT,GCT | P1456A | NP_870998.2 |
| XM_011527171.2 | 5284 | Missense Mutation | CCT,GCT | P1456A | XP_011525473.1 |
| XM_017027046.1 | 5284 | Missense Mutation | CCT,GCT | P1422A | XP_016882535.1 |
| XM_017027047.1 | 5284 | Missense Mutation | CCT,GCT | P1422A | XP_016882536.1 |