ENST00000452035.7:n.2102T>G
|
|
|
ENST00000483004.2:c.1494T>G
|
ENSP00000419887.2:p.Pro498=
|
|
ENST00000698628.1:c.1624+301T>G
|
ENSP00000513848.1:n.1624+301T>G
|
|
ENST00000698629.1:n.1887T>G
|
|
|
ENST00000698630.1:n.2426T>G
|
|
|
ENST00000698631.1:n.2427T>G
|
|
|
ENST00000698632.1:n.3221T>G
|
|
|
ENST00000698633.1:n.3111T>G
|
|
|
ENST00000698636.1:n.1932T>G
|
|
|
ENST00000425368.7:c.1710T>G
MANE Select
|
ENSP00000416561.2:p.Pro570=
|
|
ENST00000425368.6:c.1710T>G
|
ENSP00000416561.2:p.Pro570=
|
|
ENST00000456570.5:c.3216T>G
|
ENSP00000410815.1:p.Pro1072=
|
|
ENST00000467360.1:n.836T>G
|
|
|
ENST00000477310.1:c.2763T>G
|
ENSP00000418996.1:p.Pro921=
|
|
ENST00000483004.1:c.332T>G
|
|
|
NM_001710.5:c.1710T>G , LRG_136t1:c.1710T>G
|
NP_001701.2:p.Pro570=
|
|
NM_001710.6:c.1710T>G
MANE Select
|
NP_001701.2:p.Pro570=
|
|