Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001204830.1 | 789 | Missense Mutation | CTT,GTT | L231V | NP_001191759.1 |
NM_015929.3 | 789 | Missense Mutation | CTT,GTT | L231V | NP_057013.1 |
NM_145197.2 | 789 | Missense Mutation | CTT,GTT | L231V | NP_660198.1 |
NM_145198.2 | 789 | Missense Mutation | CTT,GTT | L231V | NP_660199.1 |
NM_145199.2 | 789 | Missense Mutation | CTT,GTT | L231V | NP_660200.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001320417.1 | 789 | Intron | NP_001307346.1 | ||
NM_001320418.1 | 789 | Intron | NP_001307347.1 | ||
NM_001320419.1 | 789 | Intron | NP_001307348.1 | ||
NM_138798.2 | 789 | Intron | NP_620153.1 | ||
XM_011510581.2 | 789 | Intron | XP_011508883.1 | ||
XM_011510582.2 | 789 | Intron | XP_011508884.1 | ||
XM_011510583.1 | 789 | Intron | XP_011508885.1 | ||
XM_017003314.1 | 789 | Intron | XP_016858803.1 | ||
XM_017003315.1 | 789 | Intron | XP_016858804.1 |