Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001042575.2 | 581 | Missense Mutation | CCC,CGC | P3R | NP_001036040.2 |
XM_011512754.1 | 581 | Missense Mutation | CCC,CGC | P32R | XP_011511056.1 |
XM_011512758.1 | 581 | Intron | XP_011511060.1 |