Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_138572.2 | 470 | Missense Mutation | CCT,CGT | P151R | NP_612639.2 |
XM_005248849.2 | 470 | Missense Mutation | CCT,CGT | P151R | XP_005248906.1 |
XM_011514296.1 | 470 | Missense Mutation | CCT,CGT | P151R | XP_011512598.1 |
XM_017010241.1 | 470 | Missense Mutation | CCT,CGT | P151R | XP_016865730.1 |
XM_017010242.1 | 470 | Missense Mutation | CCT,CGT | P88R | XP_016865731.1 |
XM_017010243.1 | 470 | Missense Mutation | CCT,CGT | P88R | XP_016865732.1 |
XM_017010244.1 | 470 | Missense Mutation | CCT,CGT | P151R | XP_016865733.1 |
XM_017010245.1 | 470 | Missense Mutation | CCT,CGT | P151R | XP_016865734.1 |