| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001256617.1 | 558 | Intron | NP_001243546.1 | ||
| NM_001256618.1 | 558 | Intron | NP_001243547.1 | ||
| NM_006659.3 | 558 | Intron | NP_006650.1 | ||
| XM_017015595.1 | 558 | Intron | XP_016871084.1 | ||
| XM_017015596.1 | 558 | Intron | XP_016871085.1 |
| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_145806.3 | 558 | Missense Mutation | ACG,ATG | T168M | NP_665805.2 |