Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001130014.1 | 305 | Intron | NP_001123486.1 | ||
NM_002781.3 | 305 | Intron | NP_002772.3 | ||
XM_011527132.2 | 305 | Missense Mutation | CCT,CGT | P59R | XP_011525434.1 |
XM_017027003.1 | 305 | Intron | XP_016882492.1 |