Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_145174.1 | 691 | Missense Mutation | CTT,GTT | L187V | NP_660157.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001204827.1 | 691 | Intron | NP_001191756.1 | ||
NM_022098.3 | 691 | Intron | NP_071381.1 |