Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001276342.1 | 214 | Missense Mutation | CAT,CCT | H22P | NP_001263271.1 |
NM_001318707.1 | 214 | UTR 5 | NP_001305636.1 | ||
NM_001318708.1 | 214 | UTR 5 | NP_001305637.1 | ||
NM_001318709.1 | 214 | Missense Mutation | CAT,CCT | H22P | NP_001305638.1 |
NM_013326.4 | 214 | Missense Mutation | CAT,CCT | H22P | NP_037458.3 |
XM_011525939.1 | 214 | UTR 5 | XP_011524241.1 | ||
XM_017025717.1 | 214 | UTR 5 | XP_016881206.1 |