Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001145018.1 | 708 | Missense Mutation | NP_001138490.1 | ||
XM_006718818.3 | 708 | Nonsense Mutation | XP_006718881.1 | ||
XM_011542763.2 | 708 | Nonsense Mutation | XP_011541065.1 | ||
XM_011542764.2 | 708 | Nonsense Mutation | XP_011541066.1 | ||
XM_011542770.2 | 708 | Nonsense Mutation | XP_011541072.1 | ||
XM_011542771.2 | 708 | Nonsense Mutation | XP_011541073.1 | ||
XM_011542772.2 | 708 | Nonsense Mutation | XP_011541074.1 | ||
XM_011542774.2 | 708 | Nonsense Mutation | XP_011541076.1 | ||
XM_017017577.1 | 708 | Nonsense Mutation | XP_016873066.1 | ||
XM_017017578.1 | 708 | UTR 3 | XP_016873067.1 | ||
XM_017017579.1 | 708 | Nonsense Mutation | XP_016873068.1 | ||
XM_017017580.1 | 708 | Missense Mutation | XP_016873069.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001168468.1 | 708 | Intron | NP_001161940.1 | ||
NM_024791.3 | 708 | Intron | NP_079067.3 | ||
XM_011543000.2 | 708 | Intron | XP_011541302.1 | ||
XM_011543001.2 | 708 | Intron | XP_011541303.1 | ||
XM_011543002.2 | 708 | Intron | XP_011541304.1 | ||
XM_011543005.2 | 708 | Intron | XP_011541307.1 | ||
XM_017018334.1 | 708 | Intron | XP_016873823.1 | ||
XM_017018335.1 | 708 | Intron | XP_016873824.1 | ||
XM_017018336.1 | 708 | Intron | XP_016873825.1 | ||
XM_017018337.1 | 708 | Intron | XP_016873826.1 |