Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001282275.1 | 372 | Intron | NP_001269204.1 | ||
NM_001282276.1 | 372 | Missense Mutation | CCC,CGC | P6R | NP_001269205.1 |
XM_006721865.3 | 372 | UTR 5 | XP_006721928.1 | ||
XM_011524747.2 | 372 | Intron | XP_011523049.1 | ||
XM_011524748.1 | 372 | Intron | XP_011523050.1 |