Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001142653.1 | 44 | Intron | NP_001136125.1 | ||
NM_001142654.1 | 44 | Intron | NP_001136126.1 | ||
NM_001261430.1 | 44 | Intron | NP_001248359.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001136042.2 | 44 | Intron | NP_001129514.2 | ||
NM_025267.3 | 44 | Intron | NP_079543.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001321381.1 | 44 | Missense Mutation | CCG,CTG | P10L | NP_001308310.1 |
NM_173079.3 | 44 | Missense Mutation | CCG,CTG | P10L | NP_775102.2 |
XM_005257078.3 | 44 | Missense Mutation | CCG,CTG | P10L | XP_005257135.1 |
XM_005257080.3 | 44 | Missense Mutation | CCG,CTG | P10L | XP_005257137.1 |