ENST00000700029.2:c.1133T>G
|
ENSP00000514759.2:p.Phe378Cys
|
|
ENST00000710265.1:c.*69T>G
|
ENSP00000518161.1:n.*69T>G
|
|
ENST00000688158.2:n.1775T>G
|
|
|
ENST00000688922.2:c.*870T>G
|
ENSP00000508742.2:n.*870T>G
|
|
ENST00000700021.1:c.995T>G
|
ENSP00000514757.1:p.Phe332Cys
|
|
ENST00000700022.1:c.*379T>G
|
ENSP00000514758.1:n.*379T>G
|
|
ENST00000700023.1:n.2198T>G
|
|
|
ENST00000700024.1:n.2432T>G
|
|
|
ENST00000706954.1:c.1040T>G
|
ENSP00000516674.1:p.Phe347Cys
|
|
ENST00000706955.1:c.*1075T>G
|
ENSP00000516675.1:n.*1075T>G
|
|
ENST00000686459.1:c.*626T>G
|
ENSP00000508909.1:n.*626T>G
|
|
ENST00000688158.1:c.*1151T>G
|
ENSP00000509254.1:n.*1151T>G
|
|
ENST00000688308.1:c.1040T>G
|
ENSP00000508752.1:p.Phe347Cys
|
|
ENST00000688922.1:c.961T>G
|
|
|
ENST00000693560.1:c.1559T>G
|
ENSP00000509861.1:p.Phe520Cys
|
|
ENST00000371953.8:c.1040T>G
MANE Select
|
ENSP00000361021.3:p.Phe347Cys
|
|
ENST00000371953.7:c.1040T>G
|
ENSP00000361021.3:p.Phe347Cys
|
|
NM_000314.5:c.1040T>G
|
NP_000305.3:p.Phe347Cys
|
|
NM_000314.6:c.1040T>G
|
NP_000305.3:p.Phe347Cys
|
|
NM_001304717.2:c.1559T>G
|
NP_001291646.2:p.Phe520Cys
|
|
NM_001304718.1:c.449T>G
|
NP_001291647.1:p.Phe150Cys
|
|
XM_006717926.2:c.995T>G
|
XP_006717989.1:p.Phe332Cys
|
|
XM_011539982.1:c.944T>G
|
XP_011538284.1:p.Phe315Cys
|
|
XR_945791.1:n.1610T>G
|
|
|
NM_000314.7:c.1040T>G
|
NP_000305.3:p.Phe347Cys
|
|
NM_001304717.5:c.1559T>G
|
NP_001291646.4:p.Phe520Cys
|
|
NM_001304718.2:c.449T>G
|
NP_001291647.1:p.Phe150Cys
|
|
NM_000314.8:c.1040T>G
MANE Select
|
NP_000305.3:p.Phe347Cys
|
|