ENST00000698352.1:c.*2542_*2551delinsCTTAAGGAGT
|
ENSP00000513675.1:n.*2542_*2551delinsCTTAAGGAGT
|
|
ENST00000698353.1:n.2865_2874delinsCTTAAGGAGT
|
|
|
ENST00000698354.1:c.*275_*284delinsCTTAAGGAGT
|
ENSP00000513676.1:n.*275_*284delinsCTTAAGGAGT
|
|
ENST00000296795.8:c.*275_*284delinsCTTAAGGAGT
MANE Select
|
ENSP00000296795.3:n.*275_*284delinsCTTAAGGAGT
|
|
ENST00000296795.7:c.*275_*284delinsCTTAAGGAGT
|
ENSP00000296795.2:n.*275_*284delinsCTTAAGGAGT
|
|
NM_003265.3:c.*275_*284delinsCTTAAGGAGT
MANE Select
|
NP_003256.1:n.*275_*284delinsCTTAAGGAGT
|
|