Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001321449.1 | 863 | UTR 3 | NP_001308378.1 | ||
NM_152358.2 | 863 | Nonsense Mutation | CGA,TGA | R216* | NP_689571.2 |
XM_011526436.2 | 863 | Missense Mutation | CCG,CTG | P206L | XP_011524738.1 |
XM_011526437.2 | 863 | Missense Mutation | CCG,CTG | P199L | XP_011524739.1 |