ENST00000379153.4:c.489+112T>A
MANE Select
|
ENSP00000368450.3:n.489+112T>A
|
|
ENST00000379153.3:c.489+112T>A
|
ENSP00000368450.3:n.489+112T>A
|
|
ENST00000612003.4:c.312+112T>A
|
ENSP00000480760.1:n.312+112T>A
|
|
NM_001040280.1:c.489+112T>A
|
NP_001035370.1:n.489+112T>A
|
|
NM_001251901.1:c.312+112T>A
|
NP_001238830.1:n.312+112T>A
|
|
NM_004233.3:c.489+112T>A
|
NP_004224.1:n.489+112T>A
|
|
NM_004233.4:c.489+112T>A
MANE Select
|
NP_004224.1:n.489+112T>A
|
|
NM_001040280.2:c.489+112T>A
|
NP_001035370.1:n.489+112T>A
|
|
NM_001040280.3:c.489+112T>A
|
NP_001035370.1:n.489+112T>A
|
|