Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_004913.2 | 3875 | Missense Mutation | CAG,CGG | Q626R | NP_004904.2 |
XM_005256329.4 | 3875 | Missense Mutation | CAG,CGG | Q627R | XP_005256386.1 |
XM_005256330.4 | 3875 | Missense Mutation | CAG,CGG | Q557R | XP_005256387.1 |
XM_005256331.2 | 3875 | Missense Mutation | CAG,CGG | Q461R | XP_005256388.1 |
XM_006721350.2 | 3875 | Missense Mutation | CAG,CGG | Q592R | XP_006721413.1 |
XM_011523476.2 | 3875 | Missense Mutation | CAG,CGG | Q626R | XP_011521778.1 |
XM_011523477.2 | 3875 | Missense Mutation | CAG,CGG | Q593R | XP_011521779.1 |
XM_011523478.2 | 3875 | Missense Mutation | CAG,CGG | Q592R | XP_011521780.1 |
XM_011523479.2 | 3875 | UTR 3 | XP_011521781.1 | ||
XM_011523480.2 | 3875 | Missense Mutation | CAG,CGG | Q557R | XP_011521782.1 |