Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_002250.2 | 1460 | Missense Mutation | CCG,CGG | P355R | NP_002241.1 |
XM_005258882.2 | 1460 | Missense Mutation | CCG,CGG | P323R | XP_005258939.1 |
XM_005258883.2 | 1460 | Missense Mutation | CCG,CGG | P292R | XP_005258940.1 |
XM_011526938.1 | 1460 | Intron | XP_011525240.1 |