|
NM_001252024.2:c.832G>A
MANE Select
|
NP_001238953.1:p.Gly278Arg
|
|
ENST00000256552.11:c.832G>A
MANE Select
|
ENSP00000256552.7:p.Gly278Arg
|
|
NM_001252020.1:c.883G>A
|
NP_001238949.1:p.Gly295Arg
|
|
NM_001252020.2:c.883G>A
|
NP_001238949.1:p.Gly295Arg
|
|
NM_001252024.1:c.832G>A
|
NP_001238953.1:p.Gly278Arg
|
|
NM_002420.5:c.766G>A
|
NP_002411.3:p.Gly256Arg
|
|
NM_002420.6:c.766G>A
|
NP_002411.3:p.Gly256Arg
|
|
ENST00000256552.10:c.832G>A
|
ENSP00000256552.6:p.Gly278Arg
|
|
ENST00000397795.6:c.766G>A
|
ENSP00000380897.2:p.Gly256Arg
|
|
ENST00000397795.7:c.766G>A
|
ENSP00000380897.2:p.Gly256Arg
|
|
ENST00000542188.5:c.883G>A
|
ENSP00000437849.1:p.Gly295Arg
|
|
ENST00000558445.5:c.766G>A
|
ENSP00000452946.1:p.Gly256Arg
|
|
ENST00000558445.6:c.883G>A
|
ENSP00000452946.2:p.Gly295Arg
|
|
ENST00000558768.5:c.553G>A
|
ENSP00000453119.2:p.Gly185Arg
|
|
ENST00000559177.5:c.427+4628G>A
|
ENSP00000453477.1:n.427+4628G>A
|
|
ENST00000559177.6:c.544+4628G>A
|
ENSP00000453477.2:n.544+4628G>A
|
|
ENST00000560658.5:c.766G>A
|
ENSP00000454077.1:p.Gly256Arg
|
|
ENST00000560801.5:c.553G>A
|
ENSP00000453644.2:p.Gly185Arg
|
|
ENST00000711434.1:c.766G>A
|
ENSP00000518752.1:p.Gly256Arg
|