| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001122890.2 | 844 | Missense Mutation | GCT,TCT | A289S | NP_001116362.1 |
| NM_001288702.1 | 844 | Missense Mutation | GCT,TCT | A295S | NP_001275631.1 |
| NM_001288703.1 | 844 | Intron | NP_001275632.1 | ||
| NM_001288704.1 | 844 | Intron | NP_001275633.1 | ||
| NM_153338.3 | 844 | Missense Mutation | GCT,TCT | A257S | NP_699169.2 |