Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001323627.1 | 865 | Missense Mutation | CCC,CTC | P276L | NP_001310556.1 |
NM_013304.2 | 865 | Missense Mutation | CCC,CTC | P276L | NP_037436.1 |
XM_005255915.1 | 865 | Missense Mutation | CCC,CTC | P276L | XP_005255972.1 |
XM_006721185.1 | 865 | Missense Mutation | CCC,CTC | P276L | XP_006721248.1 |
XM_011523058.1 | 865 | Missense Mutation | CCC,CTC | P276L | XP_011521360.1 |
XM_011523059.1 | 865 | Missense Mutation | CCC,CTC | P276L | XP_011521361.1 |
XM_011523060.1 | 865 | Missense Mutation | CCC,CTC | P191L | XP_011521362.1 |