Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001319292.1 | 1931 | Intron | NP_001306221.1 | ||
NM_152640.4 | 1931 | Missense Mutation | CCC,CTC | P569L | NP_689853.3 |
XM_011520927.2 | 1931 | Missense Mutation | CCC,CTC | P467L | XP_011519229.1 |