|
NM_001252024.2:c.3563A>T
MANE Select
|
NP_001238953.1:p.His1188Leu
|
|
ENST00000256552.11:c.3563A>T
MANE Select
|
ENSP00000256552.7:p.His1188Leu
|
|
NM_001252020.1:c.3614A>T
|
NP_001238949.1:p.His1205Leu
|
|
NM_001252020.2:c.3614A>T
|
NP_001238949.1:p.His1205Leu
|
|
NM_001252024.1:c.3563A>T
|
NP_001238953.1:p.His1188Leu
|
|
NM_002420.5:c.3497A>T
|
NP_002411.3:p.His1166Leu
|
|
NM_002420.6:c.3497A>T
|
NP_002411.3:p.His1166Leu
|
|
ENST00000256552.10:c.3563A>T
|
ENSP00000256552.6:p.His1188Leu
|
|
ENST00000397795.6:c.3497A>T
|
ENSP00000380897.2:p.His1166Leu
|
|
ENST00000397795.7:c.3497A>T
|
ENSP00000380897.2:p.His1166Leu
|
|
ENST00000542188.5:c.3614A>T
|
ENSP00000437849.1:p.His1205Leu
|
|
ENST00000558445.5:c.3497A>T
|
ENSP00000452946.1:p.His1166Leu
|
|
ENST00000558445.6:c.3614A>T
|
ENSP00000452946.2:p.His1205Leu
|
|
ENST00000558768.5:c.3266A>T
|
ENSP00000453119.2:p.His1089Leu
|
|
ENST00000559177.5:c.842A>T
|
ENSP00000453477.1:p.His281Leu
|
|
ENST00000559177.6:c.959A>T
|
ENSP00000453477.2:p.His320Leu
|
|
ENST00000560801.5:c.3139A>T
|
ENSP00000453644.2:n.3139A>T
|
|
ENST00000711434.1:c.3515A>T
|
ENSP00000518752.1:p.His1172Leu
|
|
XR_001751769.1:n.18T>A
|
|