ENST00000378482.7:c.527T>G
MANE Select
|
ENSP00000367743.2:p.Met176Arg
|
|
ENST00000286824.6:c.578T>G
|
ENSP00000286824.6:p.Met193Arg
|
|
ENST00000378482.6:c.527T>G
|
ENSP00000367743.2:p.Met176Arg
|
|
ENST00000419600.3:n.471T>G
|
|
|
ENST00000465127.1:c.617T>G
|
ENSP00000417050.1:p.Met206Arg
|
|
ENST00000471410.5:c.*553T>G
|
ENSP00000419290.1:n.*553T>G
|
|
ENST00000475216.5:c.*520T>G
|
ENSP00000418586.1:n.*520T>G
|
|
ENST00000488893.5:n.710T>G
|
|
|
NM_004615.3:c.527T>G
|
NP_004606.2:p.Met176Arg
|
|
NM_004615.4:c.527T>G
MANE Select
|
NP_004606.2:p.Met176Arg
|
|