| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001290033.1 | 1638 | Intron | NP_001276962.1 | ||
| NM_012133.5 | 1638 | Intron | NP_036265.3 |
| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001304968.1 | 1638 | Missense Mutation | AGG,AGT | R262S | NP_001291897.1 |
| NM_052933.3 | 1638 | Missense Mutation | AGG,AGT | R262S | NP_443165.1 |