Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001324080.1 | 362 | Intron | NP_001311009.1 | ||
NM_207468.2 | 362 | Intron | NP_997351.2 | ||
XM_017001279.1 | 362 | Intron | XP_016856768.1 | ||
XM_017001280.1 | 362 | Intron | XP_016856769.1 | ||
XM_017001281.1 | 362 | Intron | XP_016856770.1 | ||
XM_017001282.1 | 362 | Intron | XP_016856771.1 | ||
XM_017001283.1 | 362 | Missense Mutation | ATG,GTG | M119V | XP_016856772.1 |
XM_017001284.1 | 362 | Missense Mutation | ATG,GTG | M119V | XP_016856773.1 |
XM_017001285.1 | 362 | Intron | XP_016856774.1 |