| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001163377.1 | 862 | Intron | NP_001156849.1 | ||
| NM_017659.3 | 862 | Missense Mutation | GCT,TCT | A188S | NP_060129.2 |
| XM_011527048.2 | 862 | Missense Mutation | GCT,TCT | A188S | XP_011525350.1 |
| XM_017026900.1 | 862 | Missense Mutation | GCT,TCT | A188S | XP_016882389.1 |