Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_173573.2 | 1578 | Silent Mutation | GCC,GCT | A478A | NP_775844.2 |
XM_011519965.2 | 1578 | Silent Mutation | GCC,GCT | A551A | XP_011518267.2 |
XM_011519967.2 | 1578 | Silent Mutation | GCC,GCT | A511A | XP_011518269.2 |
XM_017017476.1 | 1578 | Missense Mutation | CCG,CTG | P573L | XP_016872965.1 |
XM_017017477.1 | 1578 | Missense Mutation | CCG,CTG | P568L | XP_016872966.1 |
XM_017017478.1 | 1578 | Missense Mutation | CCG,CTG | P505L | XP_016872967.1 |
XM_017017479.1 | 1578 | Silent Mutation | GCC,GCT | A551A | XP_016872968.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_198075.3 | 1578 | Intron | NP_932341.1 | ||
XM_005252775.2 | 1578 | Intron | XP_005252832.1 | ||
XM_005252776.2 | 1578 | Intron | XP_005252833.1 | ||
XM_006718132.2 | 1578 | Intron | XP_006718195.1 | ||
XM_006718133.2 | 1578 | Intron | XP_006718196.1 | ||
XM_011519875.2 | 1578 | Intron | XP_011518177.1 | ||
XM_011519876.1 | 1578 | Intron | XP_011518178.1 | ||
XM_011519877.2 | 1578 | Intron | XP_011518179.1 | ||
XM_017017167.1 | 1578 | Intron | XP_016872656.1 | ||
XM_017017168.1 | 1578 | Intron | XP_016872657.1 |