Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001103149.1 | 1611 | Intron | NP_001096619.1 | ||
NM_018215.3 | 1611 | Missense Mutation | CGT,TGT | R431C | NP_060685.2 |
XM_011527067.2 | 1611 | Missense Mutation | CGT,TGT | R431C | XP_011525369.1 |