ENST00000452035.7:n.1821T>C
|
|
|
ENST00000483004.2:c.1409-196T>C
|
ENSP00000419887.2:n.1409-196T>C
|
|
ENST00000698628.1:c.1624+20T>C
|
ENSP00000513848.1:n.1624+20T>C
|
|
ENST00000698629.1:n.1801+20T>C
|
|
|
ENST00000698630.1:n.2340+20T>C
|
|
|
ENST00000698631.1:n.2341+20T>C
|
|
|
ENST00000698632.1:n.2940T>C
|
|
|
ENST00000698633.1:n.2830T>C
|
|
|
ENST00000698636.1:n.1846+20T>C
|
|
|
ENST00000425368.7:c.1624+20T>C
MANE Select
|
ENSP00000416561.2:n.1624+20T>C
|
|
ENST00000425368.6:c.1624+20T>C
|
ENSP00000416561.2:n.1624+20T>C
|
|
ENST00000452035.6:n.1644T>C
|
|
|
ENST00000456570.5:c.3130+20T>C
|
ENSP00000410815.1:n.3130+20T>C
|
|
ENST00000467360.1:n.555T>C
|
|
|
ENST00000477310.1:c.2677+20T>C
|
ENSP00000418996.1:n.2677+20T>C
|
|
ENST00000483004.1:c.247-196T>C
|
|
|
NM_001710.5:c.1624+20T>C , LRG_136t1:c.1624+20T>C
|
NP_001701.2:n.1624+20T>C
|
|
NM_001710.6:c.1624+20T>C
MANE Select
|
NP_001701.2:n.1624+20T>C
|
|