| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_012283.1 | 815 | Intron | NP_036415.1 |
| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001146343.1 | 815 | UTR 3 | NP_001139815.1 | ||
| NM_001146345.1 | 815 | Missense Mutation | CCG,CTG | P240L | NP_001139817.1 |
| NM_025078.4 | 815 | Missense Mutation | CCG,CTG | P258L | NP_079354.2 |
| XM_005266770.2 | 815 | UTR 3 | XP_005266827.1 | ||
| XM_011526188.1 | 815 | Missense Mutation | CCG,CTG | P140L | XP_011524490.1 |
| XM_017025997.1 | 815 | Missense Mutation | CCG,CTG | P283L | XP_016881486.1 |
| XM_017025998.1 | 815 | Missense Mutation | CCG,CTG | P265L | XP_016881487.1 |
| XM_017025999.1 | 815 | Intron | XP_016881488.1 | ||
| XM_017026000.1 | 815 | Intron | XP_016881489.1 | ||
| XM_017026001.1 | 815 | Missense Mutation | CCG,CTG | P177L | XP_016881490.1 |
| XM_017026002.1 | 815 | Intron | XP_016881491.1 | ||
| XM_017026003.1 | 815 | UTR 3 | XP_016881492.1 | ||
| XM_017026004.1 | 815 | UTR 3 | XP_016881493.1 | ||
| XM_017026005.1 | 815 | Missense Mutation | CCG,CTG | P140L | XP_016881494.1 |