Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_174898.2 | 439 | Missense Mutation | CAA,GAA | Q69E | NP_777558.1 |
XM_005263869.2 | 439 | Missense Mutation | CAA,GAA | Q69E | XP_005263926.1 |
XM_005263870.3 | 439 | Missense Mutation | CAA,GAA | Q69E | XP_005263927.1 |
XM_005263871.4 | 439 | Missense Mutation | CAA,GAA | Q69E | XP_005263928.1 |
XM_011510580.2 | 439 | Missense Mutation | CAA,GAA | Q69E | XP_011508882.1 |
XM_017003311.1 | 439 | Missense Mutation | CAA,GAA | Q69E | XP_016858800.1 |
XM_017003312.1 | 439 | Missense Mutation | CAA,GAA | Q69E | XP_016858801.1 |
XM_017003313.1 | 439 | Missense Mutation | CAA,GAA | Q69E | XP_016858802.1 |