Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_002077.3 | 2345 | Missense Mutation | CCT,CTT | P679L | NP_002068.1 |
XM_005251929.3 | 2345 | Missense Mutation | CCT,CTT | P679L | XP_005251986.1 |
XM_006717062.3 | 2345 | Missense Mutation | CCT,CTT | P679L | XP_006717125.1 |
XM_006717063.3 | 2345 | Missense Mutation | CCT,CTT | P679L | XP_006717126.1 |