Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001251877.1 | 2523 | Intron | NP_001238806.1 | ||
NM_003363.3 | 2523 | Missense Mutation | CCT,CTT | P862L | NP_003354.2 |
NM_199443.2 | 2523 | Missense Mutation | CCT,CTT | P815L | NP_955475.1 |