Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001024683.1 | 508 | Missense Mutation | CCT,GCT | P126A | NP_001019854.1 |
NM_145271.3 | 508 | Missense Mutation | CCT,GCT | P140A | NP_660314.1 |
XM_005255139.2 | 508 | Missense Mutation | CCT,GCT | P63A | XP_005255196.1 |
XM_005255140.2 | 508 | Missense Mutation | CCT,GCT | P63A | XP_005255197.1 |