Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001142370.1 | 509 | Intron | NP_001135842.1 | ||
NM_014369.3 | 509 | Missense Mutation | CAG,CGG | Q138R | NP_055184.2 |
XM_006712416.3 | 509 | Intron | XP_006712479.1 | ||
XM_006712417.1 | 509 | Missense Mutation | CAG,CGG | Q138R | XP_006712480.1 |
XM_017003798.1 | 509 | Intron | XP_016859287.1 |