Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_018665.2 | 417 | Missense Mutation | CGA,GGA | R25G | NP_061135.2 |
XM_011535926.1 | 417 | Missense Mutation | CGA,GGA | R25G | XP_011534228.1 |
XM_011535927.2 | 417 | Intron | XP_011534229.1 | ||
XM_011535928.2 | 417 | UTR 5 | XP_011534230.1 | ||
XM_017011003.1 | 417 | UTR 5 | XP_016866492.1 |