Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001011537.2 | 275 | Intron | NP_001011537.2 | ||
NM_032288.6 | 275 | Missense Mutation | CCG,CGG | P19R | NP_115664.2 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001145642.3 | 275 | Intron | NP_001139114.1 | ||
NM_014687.2 | 275 | Intron | NP_055502.1 | ||
XM_005269374.3 | 275 | Intron | XP_005269431.1 | ||
XM_006713827.3 | 275 | Intron | XP_006713890.1 | ||
XM_006713828.3 | 275 | Intron | XP_006713891.1 | ||
XM_006713829.3 | 275 | Intron | XP_006713892.1 | ||
XM_006713830.3 | 275 | Intron | XP_006713893.1 | ||
XM_006713831.3 | 275 | Intron | XP_006713894.1 | ||
XM_017007543.1 | 275 | Intron | XP_016863032.1 | ||
XM_017007544.1 | 275 | Intron | XP_016863033.1 | ||
XM_017007545.1 | 275 | Intron | XP_016863034.1 |