| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001103149.1 | 1587 | Intron | NP_001096619.1 | ||
| NM_018215.3 | 1587 | Missense Mutation | GCC,TCC | A423S | NP_060685.2 |
| XM_011527067.2 | 1587 | Missense Mutation | GCC,TCC | A423S | XP_011525369.1 |