Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001169126.1 | 372 | Missense Mutation | CCG,CTG | P225L | NP_001162597.1 |
NM_001308232.1 | 372 | Missense Mutation | CCG,CTG | P109L | NP_001295161.1 |
NM_144615.2 | 372 | Missense Mutation | CCG,CTG | P229L | NP_653216.2 |
XM_017026284.1 | 372 | Intron | XP_016881773.1 |