Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_005760.2 | 190 | Intron | NP_005751.2 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001083946.1 | 190 | Missense Mutation | CCG,GCG | P39A | NP_001077415.1 |
NM_144736.4 | 190 | Missense Mutation | CCG,GCG | P39A | NP_653337.1 |
XM_005264410.1 | 190 | UTR 5 | XP_005264467.1 | ||
XM_005264411.1 | 190 | Missense Mutation | CCG,GCG | P39A | XP_005264468.1 |
XM_011532956.1 | 190 | UTR 5 | XP_011531258.1 |