ENST00000297784.10:c.1869G>A
MANE Select
|
ENSP00000297784.6:p.Glu623=
|
|
ENST00000644967.1:c.*309G>A
|
ENSP00000496159.1:n.*309G>A
|
|
ENST00000645053.1:c.1258-5922G>A
|
ENSP00000493838.1:n.1258-5922G>A
|
|
ENST00000645208.2:c.1869G>A
|
ENSP00000494684.1:p.Glu623=
|
|
ENST00000645773.1:c.1743G>A
|
ENSP00000493698.1:p.Glu581=
|
|
ENST00000645787.1:n.2012G>A
|
|
|
ENST00000646619.1:c.1431G>A
|
ENSP00000493726.1:p.Glu477=
|
|
ENST00000651183.1:c.1431G>A
|
ENSP00000498723.1:p.Glu477=
|
|
ENST00000297784.9:c.1869G>A
|
ENSP00000297784.5:p.Glu623=
|
|
ENST00000340019.4:c.1869G>A
|
ENSP00000341433.3:p.Glu623=
|
|
ENST00000469455.1:n.350G>A
|
|
|
ENST00000486417.5:n.767G>A
|
|
|
NM_138691.2:c.1869G>A
|
NP_619636.2:p.Glu623=
|
|
XM_011518213.1:c.2457G>A
|
XP_011516515.1:p.Glu819=
|
|
XM_017014256.1:c.1872G>A
|
XP_016869745.1:p.Glu624=
|
|
NM_138691.3:c.1869G>A
MANE Select
|
NP_619636.2:p.Glu623=
|
|