| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001014434.1 | 492 | Intron | NP_001014434.1 | ||
| NM_020204.2 | 492 | Missense Mutation | ACC,GCC | T19A | NP_064589.2 |
| XM_005245350.3 | 492 | Intron | XP_005245407.2 | ||
| XM_011509781.2 | 492 | Intron | XP_011508083.2 | ||
| XM_017001849.1 | 492 | Intron | XP_016857338.1 |