Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001015881.1 | 335 | Intron | NP_001015881.1 | ||
NM_001318468.1 | 335 | Intron | NP_001305397.1 | ||
NM_001318470.1 | 335 | Intron | NP_001305399.1 | ||
NM_004089.3 | 335 | Missense Mutation | CTT,TTT | L29F | NP_004080.2 |
NM_198057.2 | 335 | Intron | NP_932174.1 | ||
XM_005262099.1 | 335 | Intron | XP_005262156.1 | ||
XM_005262100.1 | 335 | Intron | XP_005262157.1 | ||
XM_005262102.1 | 335 | Intron | XP_005262159.1 | ||
XM_005262103.3 | 335 | Intron | XP_005262160.1 | ||
XM_011530884.1 | 335 | Intron | XP_011529186.1 | ||
XM_017029335.1 | 335 | Intron | XP_016884824.1 |