Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001257970.1 | 2313 | Missense Mutation | GAC,GGC | D689G | NP_001244899.1 |
NM_024110.4 | 2313 | Missense Mutation | GAC,GGC | D689G | NP_077015.2 |
NM_052819.2 | 2313 | Intron | NP_438170.1 | ||
XM_011525212.1 | 2313 | Missense Mutation | GAC,GGC | D689G | XP_011523514.1 |
XM_011525213.1 | 2313 | Missense Mutation | GAC,GGC | D689G | XP_011523515.1 |
XM_011525215.1 | 2313 | Missense Mutation | GAC,GGC | D689G | XP_011523517.1 |
XM_011525216.1 | 2313 | Missense Mutation | GAC,GGC | D689G | XP_011523518.1 |
XM_011525217.1 | 2313 | Missense Mutation | GAC,GGC | D689G | XP_011523519.1 |
XM_011525218.2 | 2313 | Missense Mutation | GAC,GGC | D689G | XP_011523520.1 |
XM_017025057.1 | 2313 | Missense Mutation | GAC,GGC | D688G | XP_016880546.1 |
XM_017025058.1 | 2313 | Intron | XP_016880547.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_000199.3 | 2313 | Intron | NP_000190.1 | ||
XM_005257582.3 | 2313 | Intron | XP_005257639.1 | ||
XM_005257583.4 | 2313 | Intron | XP_005257640.1 | ||
XM_011525126.1 | 2313 | Intron | XP_011523428.1 | ||
XM_011525127.2 | 2313 | Intron | XP_011523429.1 | ||
XM_017024951.1 | 2313 | Intron | XP_016880440.1 | ||
XM_017024952.1 | 2313 | Intron | XP_016880441.1 |