Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001145166.1 | 280 | Intron | NP_001138638.1 | ||
NM_001145167.1 | 280 | Intron | NP_001138639.1 | ||
NM_005788.3 | 280 | Silent Mutation | CTC,CTG | L21L | NP_005779.1 |
XM_011519836.2 | 280 | Intron | XP_011518138.1 | ||
XM_017017081.1 | 280 | Missense Mutation | TCC,TGC | S5C | XP_016872570.1 |