ENST00000378482.7:c.542G>A
MANE Select
|
ENSP00000367743.2:p.Cys181Tyr
|
|
ENST00000286824.6:c.593G>A
|
ENSP00000286824.6:p.Cys198Tyr
|
|
ENST00000378482.6:c.542G>A
|
ENSP00000367743.2:p.Cys181Tyr
|
|
ENST00000419600.3:n.486G>A
|
|
|
ENST00000465127.1:c.632G>A
|
ENSP00000417050.1:p.Cys211Tyr
|
|
ENST00000471410.5:c.*568G>A
|
ENSP00000419290.1:n.*568G>A
|
|
ENST00000475216.5:c.*535G>A
|
ENSP00000418586.1:n.*535G>A
|
|
ENST00000488893.5:n.725G>A
|
|
|
NM_004615.3:c.542G>A
|
NP_004606.2:p.Cys181Tyr
|
|
NM_004615.4:c.542G>A
MANE Select
|
NP_004606.2:p.Cys181Tyr
|
|