| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_000779.3 | 160 | Missense Mutation | AGC,GGC | S25G | NP_000770.2 |
| NM_001099772.1 | 160 | Missense Mutation | AGC,GGC | S25G | NP_001093242.1 |
| NM_001319161.1 | 160 | Missense Mutation | AGC,GGC | S25G | NP_001306090.1 |
| NM_001319162.1 | 160 | UTR 5 | NP_001306091.1 | ||
| NM_001319163.1 | 160 | UTR 5 | NP_001306092.1 | ||
| XM_011540832.1 | 160 | Missense Mutation | AGC,GGC | S25G | XP_011539134.1 |
| XM_011540833.1 | 160 | Intron | XP_011539135.1 | ||
| XM_017000466.1 | 160 | Missense Mutation | AGC,GGC | S25G | XP_016855955.1 |