Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001174097.2 | 877 | Missense Mutation | CCA,CTA | P217L | NP_001167568.1 |
NM_001315537.1 | 877 | Intron | NP_001302466.1 | ||
NM_002300.7 | 877 | Intron | NP_002291.1 | ||
XM_006719074.2 | 877 | Missense Mutation | CCA,CTA | P217L | XP_006719137.1 |