ENST00000674537.2:c.289C>T
|
ENSP00000502725.1:p.His97Tyr
|
|
ENST00000392302.7:c.289C>T
|
ENSP00000376120.3:p.His97Tyr
|
|
ENST00000497019.7:c.289C>T
|
ENSP00000436804.2:p.His97Tyr
|
|
ENST00000524377.7:c.451C>T
MANE Select
|
ENSP00000431418.1:p.His151Tyr
|
|
ENST00000674537.1:c.289C>T
|
ENSP00000502725.1:p.His97Tyr
|
|
ENST00000358660.3:c.451C>T
|
ENSP00000351486.3:p.His151Tyr
|
|
ENST00000368196.7:c.451C>T
|
ENSP00000357179.3:p.His151Tyr
|
|
ENST00000392302.6:c.361C>T
|
ENSP00000376120.2:p.His121Tyr
|
|
ENST00000489021.6:n.313-5507C>T
|
|
|
ENST00000497019.6:c.361C>T
|
ENSP00000436804.1:p.His121Tyr
|
|
ENST00000524377.5:c.451C>T
|
ENSP00000431418.1:p.His151Tyr
|
|
ENST00000530298.5:n.509C>T
|
|
|
NM_001007792.1:c.361C>T , LRG_261t1:c.361C>T
|
NP_001007793.1:p.His121Tyr
|
|
NM_001012331.1:c.451C>T , LRG_261t2:c.451C>T
|
NP_001012331.1:p.His151Tyr
|
|
NM_002529.3:c.451C>T , LRG_261t3:c.451C>T
|
NP_002520.2:p.His151Tyr
|
|
NM_001012331.2:c.451C>T
|
NP_001012331.1:p.His151Tyr
|
|
NM_002529.4:c.451C>T
MANE Select
|
NP_002520.2:p.His151Tyr
|
|