Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_021167.4 | 3616 | Intron | NP_066990.3 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_000466.2 | 3616 | Missense Mutation | CCT,CGT | P1162R | NP_000457.1 |
NM_001282677.1 | 3616 | Missense Mutation | CCT,CGT | P1105R | NP_001269606.1 |
NM_001282678.1 | 3616 | Missense Mutation | CCT,CGT | P954R | NP_001269607.1 |
XM_017012319.1 | 3616 | Missense Mutation | CCT,CGT | P579R | XP_016867808.1 |