ENST00000696502.1:c.4836C>G
|
ENSP00000512668.1:p.His1612Gln
|
|
ENST00000696503.1:c.4698C>G
|
ENSP00000512669.1:p.His1566Gln
|
|
ENST00000696504.1:c.4698C>G
|
ENSP00000512670.1:p.His1566Gln
|
|
ENST00000676179.1:c.4773C>G
MANE Select
|
ENSP00000502065.1:p.His1591Gln
|
|
ENST00000263934.10:c.4635C>G
|
ENSP00000263934.6:p.His1545Gln
|
|
ENST00000377081.5:c.4773C>G
|
ENSP00000366284.1:p.His1591Gln
|
|
ENST00000377086.5:c.4773C>G
|
ENSP00000366290.1:p.His1591Gln
|
|
ENST00000470616.1:n.504C>G
|
|
|
ENST00000620295.2:c.4731C>G
|
ENSP00000478500.1:p.His1577Gln
|
|
ENST00000622724.3:c.4695C>G
|
ENSP00000480063.1:p.His1565Gln
|
|
ENST00000635499.1:c.818C>G
|
|
|
NM_015074.3:c.4635C>G , LRG_252t1:c.4635C>G
|
NP_055889.2:p.His1545Gln
|
|
NM_001365951.1:c.4773C>G
|
NP_001352880.1:p.His1591Gln
|
|
NM_001365952.1:c.4773C>G
|
NP_001352881.1:p.His1591Gln
|
|
NM_001365951.3:c.4773C>G
MANE Select
|
NP_001352880.1:p.His1591Gln
|
|