| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_152243.2 | 462 | Intron | NP_689449.1 | ||
| XM_006724107.1 | 462 | Intron | XP_006724170.1 | ||
| XM_006724108.1 | 462 | Intron | XP_006724171.1 | ||
| XM_006724109.1 | 462 | Intron | XP_006724172.1 | ||
| XM_017028541.1 | 462 | Intron | XP_016884030.1 |
| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_006498.2 | 462 | Missense Mutation | CCG,CTG | P117L | NP_006489.1 |