| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001024912.2 | 1300 | UTR 3 | NP_001020083.1 | ||
| NM_001184813.1 | 1300 | Missense Mutation | CCT,TCT | P389S | NP_001171742.1 |
| NM_001184815.1 | 1300 | Missense Mutation | CCT,TCT | P420S | NP_001171744.1 |
| NM_001184816.1 | 1300 | UTR 3 | NP_001171745.1 | ||
| NM_001205344.1 | 1300 | Silent Mutation | CAC,CAT | H465H | NP_001192273.1 |
| NM_001712.4 | 1300 | Missense Mutation | CCT,TCT | P485S | NP_001703.2 |
| XM_011527206.1 | 1300 | Intron | XP_011525508.1 |