Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_013281.3 | 2561 | Missense Mutation | CTC,GTC | L466V | NP_037413.1 |
NM_198391.2 | 2561 | Missense Mutation | CTC,GTC | L466V | NP_938205.1 |
XM_005260682.4 | 2561 | Missense Mutation | CTC,GTC | L466V | XP_005260739.1 |
XM_011529204.2 | 2561 | Missense Mutation | CTC,GTC | L466V | XP_011527506.1 |
XM_011529205.2 | 2561 | Missense Mutation | CTC,GTC | L466V | XP_011527507.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001033087.1 | 2561 | Intron | NP_001028259.1 | ||
NM_080676.5 | 2561 | Intron | NP_542407.2 | ||
XM_017027675.1 | 2561 | Intron | XP_016883164.1 | ||
XM_017027676.1 | 2561 | Intron | XP_016883165.1 | ||
XM_017027677.1 | 2561 | Intron | XP_016883166.1 |