ENST00000452035.7:n.1843C>A
|
|
|
ENST00000483004.2:c.1409-174C>A
|
ENSP00000419887.2:n.1409-174C>A
|
|
ENST00000698628.1:c.1624+42C>A
|
ENSP00000513848.1:n.1624+42C>A
|
|
ENST00000698629.1:n.1801+42C>A
|
|
|
ENST00000698630.1:n.2340+42C>A
|
|
|
ENST00000698631.1:n.2341+42C>A
|
|
|
ENST00000698632.1:n.2962C>A
|
|
|
ENST00000698633.1:n.2852C>A
|
|
|
ENST00000698636.1:n.1846+42C>A
|
|
|
ENST00000425368.7:c.1624+42C>A
MANE Select
|
ENSP00000416561.2:n.1624+42C>A
|
|
ENST00000425368.6:c.1624+42C>A
|
ENSP00000416561.2:n.1624+42C>A
|
|
ENST00000452035.6:n.1666C>A
|
|
|
ENST00000456570.5:c.3130+42C>A
|
ENSP00000410815.1:n.3130+42C>A
|
|
ENST00000467360.1:n.577C>A
|
|
|
ENST00000477310.1:c.2677+42C>A
|
ENSP00000418996.1:n.2677+42C>A
|
|
ENST00000483004.1:c.247-174C>A
|
|
|
NM_001710.5:c.1624+42C>A , LRG_136t1:c.1624+42C>A
|
NP_001701.2:n.1624+42C>A
|
|
NM_001710.6:c.1624+42C>A
MANE Select
|
NP_001701.2:n.1624+42C>A
|
|