ENST00000676179.1:c.*1899C>A
MANE Select
|
ENSP00000502065.1:n.*1899C>A
|
|
ENST00000377081.5:c.*84C>A
|
ENSP00000366284.1:n.*84C>A
|
|
ENST00000377086.5:c.*1899C>A
|
ENSP00000366290.1:n.*1899C>A
|
|
ENST00000620295.2:c.5514C>A
|
ENSP00000478500.1:n.5514C>A
|
|
ENST00000622724.3:c.5478C>A
|
ENSP00000480063.1:n.5478C>A
|
|
NM_015074.3:c.*1899C>A , LRG_252t1:c.*1899C>A
|
NP_055889.2:n.*1899C>A
|
|
NM_001365951.1:c.*1899C>A
|
NP_001352880.1:n.*1899C>A
|
|
NM_001365952.1:c.*1899C>A
|
NP_001352881.1:n.*1899C>A
|
|
NM_001365951.3:c.*1899C>A
MANE Select
|
NP_001352880.1:n.*1899C>A
|
|