Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_000018.3 | 1255 | Intron | NP_000009.1 | ||
NM_001033859.2 | 1255 | Intron | NP_001029031.1 | ||
NM_001270447.1 | 1255 | Intron | NP_001257376.1 | ||
NM_001270448.1 | 1255 | Intron | NP_001257377.1 | ||
XM_006721516.2 | 1255 | Intron | XP_006721579.2 | ||
XM_011523829.1 | 1255 | Intron | XP_011522131.1 | ||
XM_011523830.1 | 1255 | Intron | XP_011522132.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001128827.2 | 1255 | Intron | NP_001122299.1 | ||
NM_001321074.1 | 1255 | Silent Mutation | CCA,CCG | P18P | NP_001308003.1 |
NM_001321075.1 | 1255 | Intron | NP_001308004.1 | ||
NM_001321076.1 | 1255 | Intron | NP_001308005.1 | ||
NM_001321077.1 | 1255 | Intron | NP_001308006.1 | ||
NM_001365.4 | 1255 | Silent Mutation | CCA,CCG | P18P | NP_001356.1 |
XM_005256491.1 | 1255 | Intron | XP_005256548.1 | ||
XM_011523698.1 | 1255 | Silent Mutation | CCA,CCG | P18P | XP_011522000.1 |
XM_011523699.2 | 1255 | Silent Mutation | CCA,CCG | P18P | XP_011522001.1 |
XM_011523702.1 | 1255 | Intron | XP_011522004.1 | ||
XM_017024288.1 | 1255 | Intron | XP_016879777.1 | ||
XM_017024289.1 | 1255 | Intron | XP_016879778.1 | ||
XM_017024290.1 | 1255 | Intron | XP_016879779.1 |