ENST00000682565.1:c.10515G>A
|
ENSP00000507671.1:p.Leu3505=
|
|
ENST00000682801.1:c.10515G>A
|
ENSP00000507862.1:p.Leu3505=
|
|
ENST00000682859.1:c.10515G>A
|
ENSP00000508222.1:p.Leu3505=
|
|
ENST00000683791.1:c.3601G>A
|
|
|
ENST00000684460.1:c.7796G>A
|
|
|
ENST00000684548.1:c.10515G>A
|
ENSP00000507421.1:p.Leu3505=
|
|
ENST00000684590.1:c.4962G>A
|
ENSP00000507376.1:p.Leu1654=
|
|
ENST00000684656.1:c.7841G>A
|
|
|
ENST00000613296.6:c.10896G>A
MANE Select
|
ENSP00000482968.1:p.Leu3632=
|
|
ENST00000651057.1:c.1050G>A
|
ENSP00000498504.1:p.Leu350=
|
|
ENST00000651434.1:c.2252G>A
|
|
|
ENST00000651750.1:c.284G>A
|
|
|
ENST00000652487.1:c.1993G>A
|
|
|
ENST00000423048.5:c.4387G>A
|
ENSP00000399833.1:n.4387G>A
|
|
ENST00000484298.5:c.10770G>A
|
ENSP00000478155.1:p.Leu3590=
|
|
ENST00000613296.4:c.10896G>A
|
ENSP00000482968.1:p.Leu3632=
|
|
ENST00000614410.4:c.10896G>A
|
ENSP00000479094.1:p.Leu3632=
|
|
ENST00000620466.4:n.4699G>A
|
|
|
NM_015120.4:c.10899G>A , LRG_741t1:c.10899G>A
|
NP_055935.4:p.Leu3633=
|
|
NM_001378454.1:c.10896G>A
MANE Select
|
NP_001365383.1:p.Leu3632=
|
|