Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001302627.1 | 8138 | Intron | NP_001289556.1 | ||
NM_025031.2 | 8138 | Intron | NP_079307.2 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_138295.3 | 8138 | Missense Mutation | CTC,TTC | L2702F | NP_612152.1 |
XM_017011798.1 | 8138 | Missense Mutation | CTC,TTC | L2761F | XP_016867287.1 |