ENST00000378482.7:c.466T>G
MANE Select
|
ENSP00000367743.2:p.Tyr156Asp
|
|
ENST00000286824.6:c.517T>G
|
ENSP00000286824.6:p.Tyr173Asp
|
|
ENST00000378482.6:c.466T>G
|
ENSP00000367743.2:p.Tyr156Asp
|
|
ENST00000419600.3:n.410T>G
|
|
|
ENST00000465127.1:c.556T>G
|
ENSP00000417050.1:p.Tyr186Asp
|
|
ENST00000471410.5:c.*492T>G
|
ENSP00000419290.1:n.*492T>G
|
|
ENST00000475216.5:c.*459T>G
|
ENSP00000418586.1:n.*459T>G
|
|
ENST00000488893.5:n.649T>G
|
|
|
NM_004615.3:c.466T>G
|
NP_004606.2:p.Tyr156Asp
|
|
NM_004615.4:c.466T>G
MANE Select
|
NP_004606.2:p.Tyr156Asp
|
|