ENST00000696502.1:c.4822C>G
|
ENSP00000512668.1:p.Gln1608Glu
|
|
ENST00000696503.1:c.4684C>G
|
ENSP00000512669.1:p.Gln1562Glu
|
|
ENST00000696504.1:c.4684C>G
|
ENSP00000512670.1:p.Gln1562Glu
|
|
ENST00000676179.1:c.4759C>G
MANE Select
|
ENSP00000502065.1:p.Gln1587Glu
|
|
ENST00000263934.10:c.4621C>G
|
ENSP00000263934.6:p.Gln1541Glu
|
|
ENST00000377081.5:c.4759C>G
|
ENSP00000366284.1:p.Gln1587Glu
|
|
ENST00000377086.5:c.4759C>G
|
ENSP00000366290.1:p.Gln1587Glu
|
|
ENST00000470616.1:n.490C>G
|
|
|
ENST00000620295.2:c.4717C>G
|
ENSP00000478500.1:p.Gln1573Glu
|
|
ENST00000622724.3:c.4681C>G
|
ENSP00000480063.1:p.Gln1561Glu
|
|
ENST00000635499.1:c.804C>G
|
|
|
NM_015074.3:c.4621C>G , LRG_252t1:c.4621C>G
|
NP_055889.2:p.Gln1541Glu
|
|
NM_001365951.1:c.4759C>G
|
NP_001352880.1:p.Gln1587Glu
|
|
NM_001365952.1:c.4759C>G
|
NP_001352881.1:p.Gln1587Glu
|
|
NM_001365951.3:c.4759C>G
MANE Select
|
NP_001352880.1:p.Gln1587Glu
|
|