Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_004286.4 | 1617 | Missense Mutation | CCG,CGG | P80R | NP_004277.2 |
XM_011530537.2 | 1617 | Missense Mutation | CCG,CGG | P80R | XP_011528839.1 |
XM_017029099.1 | 1617 | Missense Mutation | CCG,CGG | P80R | XP_016884588.1 |
XM_017029100.1 | 1617 | Missense Mutation | CCG,CGG | P80R | XP_016884589.1 |
XM_017029101.1 | 1617 | Missense Mutation | CGC,GGC | R6G | XP_016884590.1 |
XM_017029102.1 | 1617 | Intron | XP_016884591.1 | ||
XM_017029103.1 | 1617 | Intron | XP_016884592.1 |