Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001012333.2 | 528 | Missense Mutation | CCC,CTC | P47L | NP_001012333.1 |
NM_001012334.2 | 528 | Missense Mutation | CCC,CTC | P47L | NP_001012334.1 |
NM_001270550.1 | 528 | Missense Mutation | CCC,CTC | P47L | NP_001257479.1 |
NM_001270551.1 | 528 | Missense Mutation | CCC,CTC | P47L | NP_001257480.1 |
NM_001270552.1 | 528 | Intron | NP_001257481.1 | ||
NM_002391.4 | 528 | Missense Mutation | CCC,CTC | P47L | NP_002382.1 |
XM_011520116.2 | 528 | Missense Mutation | CCC,CTC | P47L | XP_011518418.1 |
XM_017017764.1 | 528 | Missense Mutation | CCC,CTC | P47L | XP_016873253.1 |