Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_003259.3 | 337 | Missense Mutation | CCC,CGC | P91R | NP_003250.3 |
XM_011528229.1 | 337 | Missense Mutation | CCC,CGC | P91R | XP_011526531.1 |
XM_017027185.1 | 337 | Intron | XP_016882674.1 |