| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001270891.1 | 449 | Missense Mutation | ACC,GCC | T142A | NP_001257820.1 |
| NM_001270892.1 | 449 | UTR 3 | NP_001257821.1 | ||
| NM_001270893.1 | 449 | UTR 3 | NP_001257822.1 | ||
| NM_024108.2 | 449 | Missense Mutation | ACC,GCC | T156A | NP_077013.1 |
| XM_017027295.1 | 449 | UTR 3 | XP_016882784.1 |