ENST00000334554.12:c.557+56T>G
MANE Select
|
ENSP00000334490.7:n.557+56T>G
|
|
ENST00000320602.11:c.384+313T>G
|
ENSP00000317804.7:n.384+313T>G
|
|
ENST00000334554.11:c.557+56T>G
|
ENSP00000334490.7:n.557+56T>G
|
|
ENST00000405930.3:c.557+56T>G
|
ENSP00000384716.3:n.557+56T>G
|
|
ENST00000468112.5:n.58-669T>G
|
|
|
ENST00000469212.5:n.12T>G
|
|
|
NM_001185024.1:c.557+56T>G
|
NP_001171953.1:n.557+56T>G
|
|
NM_013373.3:c.557+56T>G
|
NP_037505.1:n.557+56T>G
|
|
XM_006724239.2:c.557+56T>G
|
XP_006724302.1:n.557+56T>G
|
|
NM_001185024.2:c.557+56T>G
|
NP_001171953.1:n.557+56T>G
|
|
NM_013373.4:c.557+56T>G
MANE Select
|
NP_037505.1:n.557+56T>G
|
|