ENST00000545399.6:c.1032+447G>T
|
ENSP00000444688.1:n.1032+447G>T
|
|
ENST00000644613.1:c.993+447G>T
|
ENSP00000494711.1:n.993+447G>T
|
|
ENST00000648268.1:c.993+447G>T
MANE Select
|
ENSP00000498113.1:n.993+447G>T
|
|
ENST00000302102.9:c.993+447G>T
|
ENSP00000302397.5:n.993+447G>T
|
|
ENST00000441343.5:c.993+447G>T
|
ENSP00000411503.1:n.993+447G>T
|
|
ENST00000485672.2:n.753G>T
|
|
|
ENST00000543770.5:c.1026+447G>T
|
ENSP00000437577.1:n.1026+447G>T
|
|
ENST00000545399.5:c.1032+447G>T
|
ENSP00000444688.1:n.1032+447G>T
|
|
ENST00000602133.5:c.903+447G>T
|
ENSP00000471581.1:n.903+447G>T
|
|
NM_001256213.1:c.1026+447G>T
|
NP_001243142.1:n.1026+447G>T
|
|
NM_001256214.1:c.1032+447G>T
|
NP_001243143.1:n.1032+447G>T
|
|
NM_152296.4:c.993+447G>T
|
NP_689509.1:n.993+447G>T
|
|
XM_011526991.1:c.903+447G>T
|
XP_011525293.1:n.903+447G>T
|
|
NM_152296.5:c.993+447G>T
MANE Select
|
NP_689509.1:n.993+447G>T
|
|
NM_001256214.2:c.1032+447G>T
|
NP_001243143.1:n.1032+447G>T
|
|
NM_001256213.2:c.1026+447G>T
|
NP_001243142.1:n.1026+447G>T
|
|