ENST00000682565.1:c.10638T>C
|
ENSP00000507671.1:p.Leu3546=
|
|
ENST00000682801.1:c.10638T>C
|
ENSP00000507862.1:p.Leu3546=
|
|
ENST00000682859.1:c.10638T>C
|
ENSP00000508222.1:p.Leu3546=
|
|
ENST00000683791.1:c.3724T>C
|
|
|
ENST00000684460.1:c.7919T>C
|
|
|
ENST00000684548.1:c.10638T>C
|
ENSP00000507421.1:p.Leu3546=
|
|
ENST00000684590.1:c.5085T>C
|
ENSP00000507376.1:p.Leu1695=
|
|
ENST00000684656.1:c.7964T>C
|
|
|
ENST00000613296.6:c.11019T>C
MANE Select
|
ENSP00000482968.1:p.Leu3673=
|
|
ENST00000651057.1:c.1173T>C
|
ENSP00000498504.1:p.Leu391=
|
|
ENST00000651434.1:c.2375T>C
|
|
|
ENST00000651750.1:c.407T>C
|
|
|
ENST00000652487.1:c.2116T>C
|
|
|
ENST00000423048.5:c.4510T>C
|
ENSP00000399833.1:n.4510T>C
|
|
ENST00000484298.5:c.10893T>C
|
ENSP00000478155.1:p.Leu3631=
|
|
ENST00000613296.4:c.11019T>C
|
ENSP00000482968.1:p.Leu3673=
|
|
ENST00000614410.4:c.11019T>C
|
ENSP00000479094.1:p.Leu3673=
|
|
ENST00000620466.4:n.4822T>C
|
|
|
NM_015120.4:c.11022T>C , LRG_741t1:c.11022T>C
|
NP_055935.4:p.Leu3674=
|
|
NM_001378454.1:c.11019T>C
MANE Select
|
NP_001365383.1:p.Leu3673=
|
|