ENST00000676179.1:c.*1810C>G
MANE Select
|
ENSP00000502065.1:n.*1810C>G
|
|
ENST00000377081.5:c.5467C>G
|
ENSP00000366284.1:p.Gln1823Glu
|
|
ENST00000377086.5:c.*1810C>G
|
ENSP00000366290.1:n.*1810C>G
|
|
ENST00000620295.2:c.5425C>G
|
ENSP00000478500.1:p.Gln1809Glu
|
|
ENST00000622724.3:c.5389C>G
|
ENSP00000480063.1:p.Gln1797Glu
|
|
NM_015074.3:c.*1810C>G , LRG_252t1:c.*1810C>G
|
NP_055889.2:n.*1810C>G
|
|
NM_001365951.1:c.*1810C>G
|
NP_001352880.1:n.*1810C>G
|
|
NM_001365952.1:c.*1810C>G
|
NP_001352881.1:n.*1810C>G
|
|
NM_001365951.3:c.*1810C>G
MANE Select
|
NP_001352880.1:n.*1810C>G
|
|