Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_052916.2 | 2024 | Missense Mutation | CAG,CGG | Q652R | NP_443148.1 |
XM_005257007.4 | 2024 | UTR 3 | XP_005257064.1 | ||
XM_011524273.2 | 2024 | Intron | XP_011522575.1 | ||
XM_017024117.1 | 2024 | Intron | XP_016879606.1 | ||
XM_017024118.1 | 2024 | Intron | XP_016879607.1 | ||
XM_017024119.1 | 2024 | Missense Mutation | CAG,CGG | Q630R | XP_016879608.1 |
XM_017024120.1 | 2024 | Intron | XP_016879609.1 |