Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_020223.3 | 887 | Missense Mutation | AGG,GGG | R216G | NP_064608.2 |
XM_017012450.1 | 887 | Missense Mutation | AGG,GGG | R216G | XP_016867939.1 |
XM_017012451.1 | 887 | Missense Mutation | AGG,GGG | R216G | XP_016867940.1 |
XM_017012452.1 | 887 | Missense Mutation | AGG,GGG | R216G | XP_016867941.1 |
XM_017012453.1 | 887 | Missense Mutation | AGG,GGG | R216G | XP_016867942.1 |
XM_017012454.1 | 887 | Missense Mutation | AGG,GGG | R216G | XP_016867943.1 |
XM_017012455.1 | 887 | Intron | XP_016867944.1 |