Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_000895.2 | 1699 | Silent Mutation | GAC,GAT | D550D | NP_000886.1 |
NM_001256643.1 | 1699 | Silent Mutation | GAC,GAT | D526D | NP_001243572.1 |
NM_001256644.1 | 1699 | Missense Mutation | CGC,TGC | R499C | NP_001243573.1 |
XM_005268871.1 | 1699 | Missense Mutation | CGC,TGC | R523C | XP_005268928.1 |
XM_011538348.1 | 1699 | Intron | XP_011536650.1 | ||
XM_011538349.2 | 1699 | Intron | XP_011536651.1 |