| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001313726.1 | 1220 | Intron | NP_001300655.1 | ||
| NM_001313727.1 | 1220 | Intron | NP_001300656.1 | ||
| NM_031418.3 | 1220 | Intron | NP_113606.2 | ||
| XM_011520282.2 | 1220 | Intron | XP_011518584.1 | ||
| XM_017018118.1 | 1220 | Intron | XP_016873607.1 | ||
| XM_017018119.1 | 1220 | Intron | XP_016873608.1 |
| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001135091.1 | 1220 | Missense Mutation | CCG,CTG | P316L | NP_001128563.1 |
| NM_001135092.1 | 1220 | Missense Mutation | CCG,CTG | P266L | NP_001128564.1 |
| NM_145650.3 | 1220 | Missense Mutation | CCG,CTG | P289L | NP_663625.2 |
| XM_017017235.1 | 1220 | Missense Mutation | CCG,CTG | P405L | XP_016872724.1 |
| XM_017017236.1 | 1220 | Missense Mutation | CCG,CTG | P355L | XP_016872725.1 |