Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001317837.1 | 663 | Missense Mutation | AGA,AGT | R42S | NP_001304766.1 |
NM_001317838.1 | 663 | Missense Mutation | AGA,AGT | R42S | NP_001304767.1 |
NM_001317839.1 | 663 | Missense Mutation | AGA,AGT | R42S | NP_001304768.1 |
NM_001317841.1 | 663 | Missense Mutation | AGA,AGT | R16S | NP_001304770.1 |
NM_001317842.1 | 663 | Missense Mutation | AGA,AGT | R16S | NP_001304771.1 |
NM_152399.3 | 663 | Missense Mutation | AGA,AGT | R42S | NP_689612.3 |
XM_005262737.2 | 663 | Missense Mutation | AGA,AGT | R42S | XP_005262794.1 |
XM_017007725.1 | 663 | Missense Mutation | AGA,AGT | R42S | XP_016863214.1 |
XM_017007726.1 | 663 | Missense Mutation | AGA,AGT | R16S | XP_016863215.1 |