Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001040125.1 | 769 | Missense Mutation | AAT,AGT | N16S | NP_001035214.1 |
NM_001040126.1 | 769 | Intron | NP_001035215.1 | ||
NM_001287531.1 | 769 | Intron | NP_001274460.1 | ||
NM_017765.2 | 769 | Missense Mutation | AAT,AGT | N16S | NP_060235.2 |
XM_005245916.2 | 769 | Missense Mutation | AAT,AGT | N16S | XP_005245973.1 |
XM_006710710.2 | 769 | UTR 5 | XP_006710773.1 | ||
XM_006710711.2 | 769 | UTR 5 | XP_006710774.1 | ||
XM_011541634.2 | 769 | Missense Mutation | AAT,AGT | N16S | XP_011539936.1 |