Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_018216.2 | 2193 | Missense Mutation | ACG,GCG | T726A | NP_060686.2 |
XM_011541708.2 | 2193 | Intron | XP_011540010.2 | ||
XM_017001633.1 | 2193 | Missense Mutation | ACG,GCG | T571A | XP_016857122.1 |