Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001008388.4 | 1508 | Silent Mutation | CCA,CCG | P61P | NP_001008389.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001100874.2 | 1508 | Missense Mutation | CGG,TGG | R456W | NP_001094344.1 |
NM_139173.3 | 1508 | Intron | NP_631912.2 | ||
XM_006714093.3 | 1508 | Intron | XP_006714156.1 | ||
XM_011531622.1 | 1508 | Intron | XP_011529924.1 | ||
XM_011531623.1 | 1508 | Intron | XP_011529925.1 |