Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_000119.2 | 1718 | Silent Mutation | CTC,CTT | L592L | NP_000110.2 |
NM_001114134.1 | 1718 | Silent Mutation | CTC,CTT | L562L | NP_001107606.1 |
XM_005254225.1 | 1718 | Silent Mutation | CTC,CTT | L527L | XP_005254282.1 |
XM_011521349.2 | 1718 | Silent Mutation | CTC,CTT | L592L | XP_011519651.1 |
XM_011521350.2 | 1718 | Silent Mutation | CTC,CTT | L592L | XP_011519652.1 |
XM_011521351.2 | 1718 | Silent Mutation | CTC,CTT | L592L | XP_011519653.1 |
XM_011521352.2 | 1718 | Silent Mutation | CTC,CTT | L580L | XP_011519654.1 |
XM_011521353.2 | 1718 | Silent Mutation | CTC,CTT | L557L | XP_011519655.1 |
XM_011521354.2 | 1718 | Silent Mutation | CTC,CTT | L407L | XP_011519656.1 |