Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_000233.3 | 1732 | Missense Mutation | CGT,TGT | R646C | NP_000224.2 |
XM_005264309.3 | 1732 | Missense Mutation | CGT,TGT | R327C | XP_005264366.1 |
XM_006712015.3 | 1732 | Missense Mutation | CGT,TGT | R336C | XP_006712078.1 |
XM_011532828.1 | 1732 | Missense Mutation | CGT,TGT | R621C | XP_011531130.1 |
XM_011532831.1 | 1732 | Missense Mutation | CGT,TGT | R434C | XP_011531133.1 |
XM_011532834.2 | 1732 | Missense Mutation | CGT,TGT | R327C | XP_011531136.1 |
XM_017004089.1 | 1732 | Missense Mutation | CGT,TGT | R561C | XP_016859578.1 |
XM_017004090.1 | 1732 | Missense Mutation | CGT,TGT | R434C | XP_016859579.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001198593.1 | 1732 | Intron | NP_001185522.1 | ||
NM_001198594.1 | 1732 | Intron | NP_001185523.1 | ||
NM_172311.2 | 1732 | Intron | NP_758515.1 |