Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_145807.2 | 1630 | Missense Mutation | CCG,CTG | P487L | NP_665806.1 |
XM_011526443.2 | 1630 | Intron | XP_011524745.1 | ||
XM_017026274.1 | 1630 | Missense Mutation | CCG,CTG | P332L | XP_016881763.1 |