Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_005173.3 | 3305 | Missense Mutation | ATG,GTG | M996V | NP_005164.2 |
NM_174953.2 | 3305 | Missense Mutation | ATG,GTG | M1049V | NP_777613.1 |
NM_174954.2 | 3305 | Silent Mutation | AAA,AAG | K1044K | NP_777614.1 |
NM_174955.2 | 3305 | Missense Mutation | AAT,AGT | N1025S | NP_777615.1 |
NM_174956.2 | 3305 | Silent Mutation | AAA,AAG | K1029K | NP_777616.1 |
NM_174957.2 | 3305 | Missense Mutation | ATG,GTG | M995V | NP_777617.1 |
NM_174958.2 | 3305 | Silent Mutation | AAA,AAG | K1029K | NP_777618.1 |
XM_011523881.2 | 3305 | Intron | XP_011522183.1 | ||
XM_011523882.2 | 3305 | Intron | XP_011522184.1 | ||
XM_011523884.2 | 3305 | Intron | XP_011522186.1 | ||
XM_011523885.1 | 3305 | Missense Mutation | AAT,AGT | N1024S | XP_011522187.1 |
XM_011523888.2 | 3305 | Silent Mutation | AAA,AAG | K1028K | XP_011522190.1 |
XM_011523889.1 | 3305 | Intron | XP_011522191.1 | ||
XM_011523892.2 | 3305 | Intron | XP_011522194.1 | ||
XM_017024692.1 | 3305 | Intron | XP_016880181.1 | ||
XM_017024693.1 | 3305 | Intron | XP_016880182.1 |