Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_003004.2 | 1088 | Missense Mutation | CCG,CTG | P220L | NP_002995.1 |
XM_005256392.3 | 1088 | Missense Mutation | CCG,CTG | P220L | XP_005256449.1 |
XM_011523588.2 | 1088 | Missense Mutation | CCG,CTG | P220L | XP_011521890.1 |