| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001193300.1 | 382 | Silent Mutation | ACA,ACG | T28T | NP_001180229.1 |
| NM_001193301.1 | 382 | Silent Mutation | ACA,ACG | T28T | NP_001180230.1 |
| NM_001193302.1 | 382 | Intron | NP_001180231.1 | ||
| NM_022367.3 | 382 | Silent Mutation | ACA,ACG | T28T | NP_071762.2 |
| XM_011509871.2 | 382 | Intron | XP_011508173.1 | ||
| XM_011509872.2 | 382 | Silent Mutation | ACA,ACG | T28T | XP_011508174.1 |
| XM_011509873.2 | 382 | Silent Mutation | ACA,ACG | T28T | XP_011508175.1 |
| XM_011509874.2 | 382 | Intron | XP_011508176.1 | ||
| XM_011509875.2 | 382 | Intron | XP_011508177.1 | ||
| XM_011509876.2 | 382 | Intron | XP_011508178.1 | ||
| XM_011509878.2 | 382 | Intron | XP_011508180.1 | ||
| XM_011509879.2 | 382 | Intron | XP_011508181.1 | ||
| XM_017002056.1 | 382 | Silent Mutation | ACA,ACG | T28T | XP_016857545.1 |
| XM_017002057.1 | 382 | UTR 5 | XP_016857546.1 |