ENST00000297784.10:c.1846G=
MANE Select
|
ENSP00000297784.6:p.Val616=
|
|
ENST00000644967.1:c.*286G=
|
ENSP00000496159.1:n.*286G=
|
|
ENST00000645053.1:c.1258-5945G=
|
ENSP00000493838.1:n.1258-5945G=
|
|
ENST00000645208.2:c.1846G=
|
ENSP00000494684.1:p.Val616=
|
|
ENST00000645773.1:c.1720G=
|
ENSP00000493698.1:p.Val574=
|
|
ENST00000645787.1:n.1989G=
|
|
|
ENST00000646619.1:c.1408G=
|
ENSP00000493726.1:p.Val470=
|
|
ENST00000651183.1:c.1408G=
|
ENSP00000498723.1:p.Val470=
|
|
ENST00000297784.9:c.1846G=
|
ENSP00000297784.5:p.Val616=
|
|
ENST00000340019.4:c.1846G=
|
ENSP00000341433.3:p.Val616=
|
|
ENST00000469455.1:n.327G=
|
|
|
ENST00000486417.5:n.744G=
|
|
|
NM_138691.2:c.1846G=
|
NP_619636.2:p.Val616=
|
|
XM_011518213.1:c.2434G=
|
XP_011516515.1:p.Val812=
|
|
XM_017014256.1:c.1849G=
|
XP_016869745.1:p.Val617=
|
|
NM_138691.3:c.1846G=
MANE Select
|
NP_619636.2:p.Val616=
|
|