Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001100818.1 | 591 | Missense Mutation | CCG,CTG | P98L | NP_001094288.1 |
NM_017933.4 | 591 | Missense Mutation | CCG,CTG | P129L | NP_060403.3 |
XM_011511384.2 | 591 | Missense Mutation | CCG,CTG | P131L | XP_011509686.1 |
XM_017004404.1 | 591 | Missense Mutation | CCG,CTG | P186L | XP_016859893.1 |
XM_017004405.1 | 591 | Missense Mutation | CCG,CTG | P149L | XP_016859894.1 |
XM_017004406.1 | 591 | Missense Mutation | CCG,CTG | P84L | XP_016859895.1 |
XM_017004407.1 | 591 | Missense Mutation | CCG,CTG | P49L | XP_016859896.1 |