| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001193529.2 | 656 | Intron | NP_001180458.1 | ||
| NM_001193530.1 | 656 | Intron | NP_001180459.1 | ||
| NM_006584.3 | 656 | Intron | NP_006575.2 | ||
| XM_011524203.2 | 656 | Intron | XP_011522505.1 | ||
| XM_017024023.1 | 656 | Intron | XP_016879512.1 | ||
| XM_017024024.1 | 656 | Intron | XP_016879513.1 |
| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_052857.3 | 656 | Missense Mutation | AAC,GAC | N207D | NP_443089.3 |