Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_174945.2 | 442 | Missense Mutation | CCG,TCG | P58S | NP_777605.1 |
XM_005258783.3 | 442 | Missense Mutation | CCG,TCG | P58S | XP_005258840.1 |
XM_011526793.2 | 442 | Missense Mutation | CCG,TCG | P58S | XP_011525095.1 |