Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001012754.3 | 397 | Missense Mutation | CGT,CTT | R23L | NP_001012772.1 |
NM_001017370.2 | 397 | Missense Mutation | CGT,CTT | R23L | NP_001017370.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_025138.4 | 397 | Intron | NP_079414.3 | ||
XM_005266545.3 | 397 | Intron | XP_005266602.1 | ||
XM_011535239.2 | 397 | Intron | XP_011533541.1 |