ENST00000682565.1:c.11668C>G
|
ENSP00000507671.1:p.Leu3890Val
|
|
ENST00000682801.1:c.11167-814C>G
|
ENSP00000507862.1:n.11167-814C>G
|
|
ENST00000682859.1:c.11668C>G
|
ENSP00000508222.1:p.Leu3890Val
|
|
ENST00000683791.1:c.4754C>G
|
|
|
ENST00000684460.1:c.8949C>G
|
|
|
ENST00000684548.1:c.11668C>G
|
ENSP00000507421.1:p.Leu3890Val
|
|
ENST00000684590.1:c.6115C>G
|
ENSP00000507376.1:p.Leu2039Val
|
|
ENST00000684656.1:c.9133C>G
|
|
|
ENST00000613296.6:c.12049C>G
MANE Select
|
ENSP00000482968.1:p.Leu4017Val
|
|
ENST00000651057.1:c.2203C>G
|
ENSP00000498504.1:p.Leu735Val
|
|
ENST00000651434.1:c.3405C>G
|
|
|
ENST00000651750.1:c.1260+490C>G
|
|
|
ENST00000652487.1:c.3220C>G
|
|
|
ENST00000464408.3:n.224C>G
|
|
|
ENST00000484298.5:c.11923C>G
|
ENSP00000478155.1:p.Leu3975Val
|
|
ENST00000613296.4:c.12049C>G
|
ENSP00000482968.1:p.Leu4017Val
|
|
ENST00000620466.4:n.5852C>G
|
|
|
NM_015120.4:c.12052C>G , LRG_741t1:c.12052C>G
|
NP_055935.4:p.Leu4018Val
|
|
NM_001378454.1:c.12049C>G
MANE Select
|
NP_001365383.1:p.Leu4017Val
|
|