| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001319292.1 | 2059 | Intron | NP_001306221.1 | ||
| NM_152640.4 | 2059 | Missense Mutation | ACC,GCC | T612A | NP_689853.3 |
| XM_011520927.2 | 2059 | Missense Mutation | ACC,GCC | T510A | XP_011519229.1 |