ENST00000378482.7:c.497T>G
MANE Select
|
ENSP00000367743.2:p.Leu166Arg
|
|
ENST00000286824.6:c.548T>G
|
ENSP00000286824.6:p.Leu183Arg
|
|
ENST00000378482.6:c.497T>G
|
ENSP00000367743.2:p.Leu166Arg
|
|
ENST00000419600.3:n.441T>G
|
|
|
ENST00000465127.1:c.587T>G
|
ENSP00000417050.1:p.Leu196Arg
|
|
ENST00000471410.5:c.*523T>G
|
ENSP00000419290.1:n.*523T>G
|
|
ENST00000475216.5:c.*490T>G
|
ENSP00000418586.1:n.*490T>G
|
|
ENST00000488893.5:n.680T>G
|
|
|
NM_004615.3:c.497T>G
|
NP_004606.2:p.Leu166Arg
|
|
NM_004615.4:c.497T>G
MANE Select
|
NP_004606.2:p.Leu166Arg
|
|