| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_004536.2 | 858 | Missense Mutation | GCA,GGA | A47G | NP_004527.2 |
| NM_022892.1 | 858 | Intron | NP_075043.1 | ||
| XM_011543413.2 | 858 | Intron | XP_011541715.1 | ||
| XM_017009490.1 | 858 | Intron | XP_016864979.1 |