| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001303135.1 | 169 | Missense Mutation | AGC,GGC | S48G | NP_001290064.1 |
| NM_006229.3 | 169 | Missense Mutation | AGC,GGC | S48G | NP_006220.1 |
| XM_011539868.1 | 169 | Missense Mutation | AGC,GGC | S48G | XP_011538170.1 |
| XM_011539869.1 | 169 | UTR 5 | XP_011538171.1 |