Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001304485.1 | 726 | Missense Mutation | TGT,TTT | C67F | NP_001291414.1 |
NM_001304486.1 | 726 | Missense Mutation | TGT,TTT | C67F | NP_001291415.1 |
NM_001304487.1 | 726 | Missense Mutation | TGT,TTT | C67F | NP_001291416.1 |
NM_001304488.1 | 726 | Intron | NP_001291417.1 | ||
NM_001304489.1 | 726 | Intron | NP_001291418.1 | ||
NM_001304490.1 | 726 | Intron | NP_001291419.1 | ||
NM_001304491.1 | 726 | Intron | NP_001291420.1 | ||
NM_012460.3 | 726 | Missense Mutation | TGT,TTT | C67F | NP_036592.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_207377.2 | 726 | Intron | NP_997260.1 | ||
XM_011536742.2 | 726 | Intron | XP_011535044.1 | ||
XM_011536743.2 | 726 | Intron | XP_011535045.1 | ||
XM_011536744.2 | 726 | Intron | XP_011535046.1 |