| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001008801.1 | 1026 | Intron | NP_001008801.1 | ||
| NM_001277120.1 | 1026 | Intron | NP_001264049.1 | ||
| XM_017027443.1 | 1026 | Missense Mutation | AGC,AGG | S239R | XP_016882932.1 |
| XM_017027444.1 | 1026 | Missense Mutation | AGC,AGG | S167R | XP_016882933.1 |