Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001037811.2 | 395 | Missense Mutation | CTC,GTC | L122V | NP_001032900.1 |
NM_004493.2 | 395 | Missense Mutation | CTC,GTC | L122V | NP_004484.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001031745.4 | 395 | Intron | NP_001026915.1 | ||
NM_001267053.3 | 395 | Intron | NP_001253982.1 | ||
NM_144968.3 | 395 | Intron | NP_659405.1 | ||
XM_005261988.3 | 395 | Intron | XP_005262045.1 | ||
XM_005261990.3 | 395 | Intron | XP_005262047.1 |