Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001276289.1 | 3437 | Intron | NP_001263218.1 | ||
NM_001276290.1 | 3437 | Intron | NP_001263219.1 | ||
NM_001278433.1 | 3437 | Intron | NP_001265362.1 | ||
NM_002734.4 | 3437 | Intron | NP_002725.1 | ||
NM_212471.2 | 3437 | Intron | NP_997636.1 | ||
NM_212472.2 | 3437 | Intron | NP_997637.1 | ||
XM_011524983.2 | 3437 | Intron | XP_011523285.1 | ||
XM_011524984.2 | 3437 | Intron | XP_011523286.1 | ||
XM_011524985.2 | 3437 | Intron | XP_011523287.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001320772.1 | 3437 | Missense Mutation | GAC,GGC | D359G | NP_001307701.1 |
NM_017983.6 | 3437 | Missense Mutation | GAC,GGC | D441G | NP_060453.3 |
XM_017024808.1 | 3437 | Missense Mutation | GAC,GGC | D313G | XP_016880297.1 |