Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001318192.1 | 2531 | Missense Mutation | CCC,CTC | P608L | NP_001305121.1 |
NM_012450.3 | 2531 | Missense Mutation | CCC,CTC | P607L | NP_036582.2 |
XM_011516024.2 | 2531 | Missense Mutation | CCC,CTC | P562L | XP_011514326.1 |
XM_017011962.1 | 2531 | Missense Mutation | CCC,CTC | P556L | XP_016867451.1 |
XM_017011963.1 | 2531 | Intron | XP_016867452.1 |