ENST00000482363.2:n.3028A>G
|
|
|
ENST00000688055.1:c.*1842A>G
|
ENSP00000508688.1:n.*1842A>G
|
|
ENST00000382564.8:c.*564A>G
MANE Select
|
ENSP00000372005.2:n.*564A>G
|
|
ENST00000382564.6:c.*564A>G
|
ENSP00000372005.2:n.*564A>G
|
|
ENST00000469657.5:c.*691A>G
|
ENSP00000418058.1:n.*691A>G
|
|
NM_001190233.1:c.*564A>G
|
NP_001177162.1:n.*564A>G
|
|
NM_145261.3:c.*564A>G
|
NP_660304.1:n.*564A>G
|
|
NR_033721.1:n.1035A>G
|
|
|
NR_033722.1:n.1007A>G
|
|
|
NR_033723.1:n.1032A>G
|
|
|
NR_046073.1:n.881A>G
|
|
|
NM_145261.4:c.*564A>G
MANE Select
|
NP_660304.1:n.*564A>G
|
|
NM_001190233.2:c.*564A>G
|
NP_001177162.1:n.*564A>G
|
|
NR_033721.2:n.997A>G
|
|
|
NR_033722.2:n.969A>G
|
|
|