ENST00000452035.7:n.1794C>G
|
|
|
ENST00000483004.2:c.1409-223C>G
|
ENSP00000419887.2:n.1409-223C>G
|
|
ENST00000698628.1:c.1617C>G
|
ENSP00000513848.1:p.Val539=
|
|
ENST00000698629.1:n.1794C>G
|
|
|
ENST00000698630.1:n.2333C>G
|
|
|
ENST00000698631.1:n.2334C>G
|
|
|
ENST00000698632.1:n.2913C>G
|
|
|
ENST00000698633.1:n.2803C>G
|
|
|
ENST00000698636.1:n.1839C>G
|
|
|
ENST00000425368.7:c.1617C>G
MANE Select
|
ENSP00000416561.2:p.Val539=
|
|
ENST00000425368.6:c.1617C>G
|
ENSP00000416561.2:p.Val539=
|
|
ENST00000452035.6:n.1617C>G
|
|
|
ENST00000456570.5:c.3123C>G
|
ENSP00000410815.1:p.Val1041=
|
|
ENST00000467360.1:n.528C>G
|
|
|
ENST00000477310.1:c.2670C>G
|
ENSP00000418996.1:p.Val890=
|
|
ENST00000483004.1:c.247-223C>G
|
|
|
NM_001710.5:c.1617C>G , LRG_136t1:c.1617C>G
|
NP_001701.2:p.Val539=
|
|
NM_001710.6:c.1617C>G
MANE Select
|
NP_001701.2:p.Val539=
|
|