Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001278506.1 | 692 | Silent Mutation | GGC,GGT | G240G | NP_001265435.1 |
NM_001323594.1 | 692 | Silent Mutation | GGC,GGT | G228G | NP_001310523.1 |
NM_001323595.1 | 692 | Silent Mutation | GGC,GGT | G251G | NP_001310524.1 |
NM_001323596.1 | 692 | Intron | NP_001310525.1 | ||
NM_001323597.1 | 692 | Silent Mutation | GGC,GGT | G202G | NP_001310526.1 |
NM_002484.3 | 692 | Silent Mutation | GGC,GGT | G251G | NP_002475.2 |
XM_017023252.1 | 692 | Silent Mutation | GGC,GGT | G228G | XP_016878741.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001079512.3 | 692 | Intron | NP_001072980.1 | ||
NM_001318873.1 | 692 | Intron | NP_001305802.1 | ||
XM_006720944.3 | 692 | Intron | XP_006721007.1 | ||
XM_011522654.2 | 692 | Intron | XP_011520956.1 | ||
XM_017023649.1 | 692 | Intron | XP_016879138.1 | ||
XM_017023650.1 | 692 | Intron | XP_016879139.1 | ||
XM_017023651.1 | 692 | Intron | XP_016879140.1 |