ENST00000674537.2:c.143G=
|
ENSP00000502725.1:p.Gly48=
|
|
ENST00000392302.7:c.143G=
|
ENSP00000376120.3:p.Gly48=
|
|
ENST00000497019.7:c.143G=
|
ENSP00000436804.2:p.Gly48=
|
|
ENST00000524377.7:c.305G=
MANE Select
|
ENSP00000431418.1:p.Gly102=
|
|
ENST00000674537.1:c.143G=
|
ENSP00000502725.1:p.Gly48=
|
|
ENST00000675461.1:c.305G=
|
ENSP00000501668.1:p.Gly102=
|
|
ENST00000358660.3:c.305G=
|
ENSP00000351486.3:p.Gly102=
|
|
ENST00000368196.7:c.305G=
|
ENSP00000357179.3:p.Gly102=
|
|
ENST00000392302.6:c.215G=
|
ENSP00000376120.2:p.Gly72=
|
|
ENST00000489021.6:n.313-8888G=
|
|
|
ENST00000497019.6:c.215G=
|
ENSP00000436804.1:p.Gly72=
|
|
ENST00000524377.5:c.305G=
|
ENSP00000431418.1:p.Gly102=
|
|
ENST00000530298.5:n.363G=
|
|
|
ENST00000533630.1:n.327G=
|
|
|
NM_001007792.1:c.215G= , LRG_261t1:c.215G=
|
NP_001007793.1:p.Gly72=
|
|
NM_001012331.1:c.305G= , LRG_261t2:c.305G=
|
NP_001012331.1:p.Gly102=
|
|
NM_002529.3:c.305G= , LRG_261t3:c.305G=
|
NP_002520.2:p.Gly102=
|
|
NM_001012331.2:c.305G=
|
NP_001012331.1:p.Gly102=
|
|
NM_002529.4:c.305G=
MANE Select
|
NP_002520.2:p.Gly102=
|
|