| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001098491.1 | 677 | Missense Mutation | TCC,TGC | S159C | NP_001091961.1 |
| NM_001098492.1 | 677 | Missense Mutation | TCC,TGC | S146C | NP_001091962.1 |
| NM_001098493.1 | 677 | Missense Mutation | TCC,TGC | S145C | NP_001091963.1 |
| NM_001098494.1 | 677 | Missense Mutation | TCC,TGC | S126C | NP_001091964.1 |
| NM_001098495.1 | 677 | Missense Mutation | TCC,TGC | S113C | NP_001091965.1 |
| NM_001098496.1 | 677 | Missense Mutation | TCC,TGC | S112C | NP_001091966.1 |
| NM_001291743.1 | 677 | Missense Mutation | TCC,TGC | S125C | NP_001278672.1 |
| NM_001291744.1 | 677 | Missense Mutation | TCC,TGC | S70C | NP_001278673.1 |
| NM_001291745.1 | 677 | Intron | NP_001278674.1 | ||
| NM_024691.3 | 677 | Missense Mutation | TCC,TGC | S158C | NP_078967.3 |