ENST00000696502.1:c.4827T>A
|
ENSP00000512668.1:p.Leu1609=
|
|
ENST00000696503.1:c.4689T>A
|
ENSP00000512669.1:p.Leu1563=
|
|
ENST00000696504.1:c.4689T>A
|
ENSP00000512670.1:p.Leu1563=
|
|
ENST00000676179.1:c.4764T>A
MANE Select
|
ENSP00000502065.1:p.Leu1588=
|
|
ENST00000263934.10:c.4626T>A
|
ENSP00000263934.6:p.Leu1542=
|
|
ENST00000377081.5:c.4764T>A
|
ENSP00000366284.1:p.Leu1588=
|
|
ENST00000377086.5:c.4764T>A
|
ENSP00000366290.1:p.Leu1588=
|
|
ENST00000470616.1:n.495T>A
|
|
|
ENST00000620295.2:c.4722T>A
|
ENSP00000478500.1:p.Leu1574=
|
|
ENST00000622724.3:c.4686T>A
|
ENSP00000480063.1:p.Leu1562=
|
|
ENST00000635499.1:c.809T>A
|
|
|
NM_015074.3:c.4626T>A , LRG_252t1:c.4626T>A
|
NP_055889.2:p.Leu1542=
|
|
NM_001365951.1:c.4764T>A
|
NP_001352880.1:p.Leu1588=
|
|
NM_001365952.1:c.4764T>A
|
NP_001352881.1:p.Leu1588=
|
|
NM_001365951.3:c.4764T>A
MANE Select
|
NP_001352880.1:p.Leu1588=
|
|