Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_021939.3 | 369 | Missense Mutation | CCC,CGC | P15R | NP_068758.3 |
XM_011525099.2 | 369 | Missense Mutation | CCC,CGC | P15R | XP_011523401.1 |
XM_011525100.2 | 369 | UTR 5 | XP_011523402.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_006455.2 | 369 | Intron | NP_006446.1 | ||
XM_006721640.3 | 369 | Intron | XP_006721703.1 |