| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_024649.4 | 1121 | Missense Mutation | CCG,CTG | P370L | NP_078925.3 |
| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_207340.1 | 1121 | Intron | NP_997223.1 | ||
| XM_005273874.3 | 1121 | Intron | XP_005273931.1 | ||
| XM_011544893.2 | 1121 | Intron | XP_011543195.1 | ||
| XM_011544894.1 | 1121 | Intron | XP_011543196.1 |