| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_015891.2 | 197 | Missense Mutation | CCG,CTG | P58L | NP_056975.1 |
| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001024934.1 | 197 | Intron | NP_001020105.1 | ||
| NM_001024935.1 | 197 | Intron | NP_001020106.1 | ||
| NM_001024936.1 | 197 | Intron | NP_001020107.1 | ||
| NM_003931.2 | 197 | Intron | NP_003922.1 | ||
| XM_005267203.3 | 197 | Intron | XP_005267260.1 | ||
| XM_005267205.2 | 197 | Intron | XP_005267262.1 | ||
| XM_005267206.2 | 197 | Intron | XP_005267263.1 | ||
| XM_005267207.2 | 197 | Intron | XP_005267264.1 | ||
| XM_011536233.1 | 197 | Intron | XP_011534535.1 | ||
| XM_011536234.1 | 197 | Intron | XP_011534536.1 | ||
| XM_011536235.1 | 197 | Intron | XP_011534537.1 | ||
| XM_017011437.1 | 197 | Intron | XP_016866926.1 | ||
| XM_017011438.1 | 197 | Intron | XP_016866927.1 | ||
| XM_017011439.1 | 197 | Intron | XP_016866928.1 | ||
| XM_017011440.1 | 197 | Intron | XP_016866929.1 | ||
| XM_017011441.1 | 197 | Intron | XP_016866930.1 | ||
| XM_017011442.1 | 197 | Intron | XP_016866931.1 | ||
| XM_017011443.1 | 197 | Intron | XP_016866932.1 | ||
| XM_017011444.1 | 197 | Intron | XP_016866933.1 |