Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_000528.3 | 2272 | Missense Mutation | ACG,CCG | T873P | NP_000519.2 |
NM_001173498.1 | 2272 | Missense Mutation | ACG,CCG | T872P | NP_001166969.1 |
XM_005259913.1 | 2272 | Missense Mutation | ACG,CCG | T874P | XP_005259970.1 |
XM_017026818.1 | 2272 | Missense Mutation | ACG,CCG | T506P | XP_016882307.1 |