Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_182502.3 | 1292 | Missense Mutation | AGC,CGC | S386R | NP_872308.2 |
XM_011531608.2 | 1292 | Missense Mutation | AGC,CGC | S386R | XP_011529910.1 |
XM_011531609.1 | 1292 | Intron | XP_011529911.1 |