ENST00000471318.6:n.909A>G
|
|
|
ENST00000621467.5:c.987A>G
|
ENSP00000480508.2:p.Leu329=
|
|
ENST00000686475.1:n.1053A>G
|
|
|
ENST00000409883.7:c.1113A>G
MANE Select
|
ENSP00000386264.2:p.Leu371=
|
|
ENST00000286196.9:c.*677A>G
|
ENSP00000286196.5:n.*677A>G
|
|
ENST00000409444.6:c.1089A>G
|
ENSP00000387203.2:p.Leu363=
|
|
ENST00000409883.6:c.1113A>G
|
ENSP00000386264.2:p.Leu371=
|
|
ENST00000471318.5:n.341A>G
|
|
|
ENST00000495329.1:n.252A>G
|
|
|
ENST00000621467.4:c.1089A>G
|
ENSP00000480508.1:p.Leu363=
|
|
NM_001044385.2:c.1113A>G
|
NP_001037850.1:p.Leu371=
|
|
NM_152388.3:c.1089A>G
|
NP_689601.2:p.Leu363=
|
|
NM_001044385.3:c.1113A>G
MANE Select
|
NP_001037850.1:p.Leu371=
|
|
NM_152388.4:c.1089A>G
|
NP_689601.2:p.Leu363=
|
|