ENST00000674537.2:c.914A>G
|
ENSP00000502725.1:p.Tyr305Cys
|
|
ENST00000392302.7:c.914A>G
|
ENSP00000376120.3:p.Tyr305Cys
|
|
ENST00000497019.7:c.781A>G
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ENSP00000436804.2:p.Thr261Ala
|
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ENST00000524377.7:c.1076A>G
MANE Select
|
ENSP00000431418.1:p.Tyr359Cys
|
|
ENST00000674537.1:c.914A>G
|
ENSP00000502725.1:p.Tyr305Cys
|
|
ENST00000358660.3:c.1076A>G
|
ENSP00000351486.3:p.Tyr359Cys
|
|
ENST00000368196.7:c.1076A>G
|
ENSP00000357179.3:p.Tyr359Cys
|
|
ENST00000392302.6:c.986A>G
|
ENSP00000376120.2:p.Tyr329Cys
|
|
ENST00000489021.6:n.538A>G
|
|
|
ENST00000497019.6:c.853A>G
|
ENSP00000436804.1:p.Thr285Ala
|
|
ENST00000524377.5:c.1076A>G
|
ENSP00000431418.1:p.Tyr359Cys
|
|
ENST00000530298.5:n.1134A>G
|
|
|
NM_001007792.1:c.986A>G , LRG_261t1:c.986A>G
|
NP_001007793.1:p.Tyr329Cys
|
|
NM_001012331.1:c.1076A>G , LRG_261t2:c.1076A>G
|
NP_001012331.1:p.Tyr359Cys
|
|
NM_002529.3:c.1076A>G , LRG_261t3:c.1076A>G
|
NP_002520.2:p.Tyr359Cys
|
|
NM_001012331.2:c.1076A>G
|
NP_001012331.1:p.Tyr359Cys
|
|
NM_002529.4:c.1076A>G
MANE Select
|
NP_002520.2:p.Tyr359Cys
|
|