Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001135050.1 | 3083 | Missense Mutation | CCC,CTC | P962L | NP_001128522.1 |
NM_020789.3 | 3083 | Missense Mutation | CCC,CTC | P946L | NP_065840.2 |
XM_017001884.1 | 3083 | Intron | XP_016857373.1 |