| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001284334.1 | 658 | Intron | NP_001271263.1 | ||
| NM_014509.4 | 658 | Intron | NP_055324.2 | ||
| XM_017028738.1 | 658 | Missense Mutation | AGC,AGG | S170R | XP_016884227.1 |
| XM_017028739.1 | 658 | Missense Mutation | AGC,AGG | S170R | XP_016884228.1 |