Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_199173.5 | 413 | Silent Mutation | GGC,GGT | G27G | NP_954642.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001272104.1 | 413 | Intron | NP_001259033.1 | ||
NM_001272105.1 | 413 | Intron | NP_001259034.1 | ||
NM_001272106.1 | 413 | Intron | NP_001259035.1 | ||
NM_001272107.1 | 413 | Intron | NP_001259036.1 | ||
NM_001272108.1 | 413 | Intron | NP_001259037.1 | ||
NM_001272109.1 | 413 | Intron | NP_001259038.1 | ||
NM_001272110.1 | 413 | Intron | NP_001259039.1 | ||
NM_001272111.1 | 413 | Intron | NP_001259040.1 | ||
NM_001272112.1 | 413 | Intron | NP_001259041.1 | ||
NM_001272113.1 | 413 | Intron | NP_001259042.1 | ||
NM_024897.3 | 413 | Intron | NP_079173.2 | ||
NM_198406.2 | 413 | Intron | NP_940798.1 | ||
XM_005245494.3 | 413 | Intron | XP_005245551.1 | ||
XM_006711546.2 | 413 | Intron | XP_006711609.1 | ||
XM_006711547.3 | 413 | Intron | XP_006711610.1 | ||
XM_006711548.3 | 413 | Intron | XP_006711611.1 | ||
XM_006711552.2 | 413 | Intron | XP_006711615.1 | ||
XM_006711553.3 | 413 | Intron | XP_006711616.1 | ||
XM_011510000.2 | 413 | Intron | XP_011508302.1 | ||
XM_017002385.1 | 413 | Intron | XP_016857874.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001199661.1 | 413 | Missense Mutation | CGC,TGC | R174C | NP_001186590.1 |
NM_001199662.1 | 413 | Missense Mutation | GCG,GTG | A194V | NP_001186591.1 |
NM_001199663.1 | 413 | Missense Mutation | CGC,TGC | R129C | NP_001186592.1 |
NM_001199664.1 | 413 | Missense Mutation | GCG,GTG | A125V | NP_001186593.1 |