| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_000179.2 | 177 | Missense Mutation | AGC,GGC | S9G | NP_000170.1 |
| NM_001281492.1 | 177 | Missense Mutation | AGC,GGC | S9G | NP_001268421.1 |
| NM_001281493.1 | 177 | UTR 5 | NP_001268422.1 | ||
| NM_001281494.1 | 177 | Intron | NP_001268423.1 | ||
| XM_011532798.1 | 177 | Intron | XP_011531100.1 | ||
| XM_011532799.1 | 177 | Intron | XP_011531101.1 |