ENST00000682565.1:c.10549C>G
|
ENSP00000507671.1:p.Leu3517Val
|
|
ENST00000682801.1:c.10549C>G
|
ENSP00000507862.1:p.Leu3517Val
|
|
ENST00000682859.1:c.10549C>G
|
ENSP00000508222.1:p.Leu3517Val
|
|
ENST00000683791.1:c.3635C>G
|
|
|
ENST00000684460.1:c.7830C>G
|
|
|
ENST00000684548.1:c.10549C>G
|
ENSP00000507421.1:p.Leu3517Val
|
|
ENST00000684590.1:c.4996C>G
|
ENSP00000507376.1:p.Leu1666Val
|
|
ENST00000684656.1:c.7875C>G
|
|
|
ENST00000613296.6:c.10930C>G
MANE Select
|
ENSP00000482968.1:p.Leu3644Val
|
|
ENST00000651057.1:c.1084C>G
|
ENSP00000498504.1:p.Leu362Val
|
|
ENST00000651434.1:c.2286C>G
|
|
|
ENST00000651750.1:c.318C>G
|
|
|
ENST00000652487.1:c.2027C>G
|
|
|
ENST00000423048.5:c.4421C>G
|
ENSP00000399833.1:n.4421C>G
|
|
ENST00000484298.5:c.10804C>G
|
ENSP00000478155.1:p.Leu3602Val
|
|
ENST00000613296.4:c.10930C>G
|
ENSP00000482968.1:p.Leu3644Val
|
|
ENST00000614410.4:c.10930C>G
|
ENSP00000479094.1:p.Leu3644Val
|
|
ENST00000620466.4:n.4733C>G
|
|
|
NM_015120.4:c.10933C>G , LRG_741t1:c.10933C>G
|
NP_055935.4:p.Leu3645Val
|
|
NM_001378454.1:c.10930C>G
MANE Select
|
NP_001365383.1:p.Leu3644Val
|
|