Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001009996.2 | 1466 | Missense Mutation | ATT,GTT | I364V | NP_001009996.1 |
NM_001276405.1 | 1466 | Missense Mutation | ATT,GTT | I364V | NP_001263334.1 |
NM_018114.5 | 1466 | Missense Mutation | ATT,GTT | I197V | NP_060584.3 |
XM_005265269.3 | 1466 | Missense Mutation | ATT,GTT | I364V | XP_005265326.1 |
XM_006713219.2 | 1466 | Missense Mutation | ATT,GTT | I197V | XP_006713282.1 |
XM_011533891.1 | 1466 | Missense Mutation | ATT,GTT | I364V | XP_011532193.1 |
XM_011533892.1 | 1466 | Missense Mutation | ATT,GTT | I197V | XP_011532194.1 |
XM_011533893.1 | 1466 | Missense Mutation | TAT,TGT | Y343C | XP_011532195.1 |
XM_017006723.1 | 1466 | Missense Mutation | ATT,GTT | I197V | XP_016862212.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001320546.1 | 1466 | Intron | NP_001307475.1 | ||
NM_001320547.1 | 1466 | Intron | NP_001307476.1 | ||
NM_018031.4 | 1466 | Intron | NP_060501.3 |