ENST00000452035.7:n.2120C>A
|
|
|
ENST00000483004.2:c.1512C>A
|
ENSP00000419887.2:p.Asp504Glu
|
|
ENST00000698628.1:c.1624+319C>A
|
ENSP00000513848.1:n.1624+319C>A
|
|
ENST00000698629.1:n.1905C>A
|
|
|
ENST00000698630.1:n.2444C>A
|
|
|
ENST00000698631.1:n.2445C>A
|
|
|
ENST00000698632.1:n.3239C>A
|
|
|
ENST00000698633.1:n.3129C>A
|
|
|
ENST00000698636.1:n.1950C>A
|
|
|
ENST00000425368.7:c.1728C>A
MANE Select
|
ENSP00000416561.2:p.Asp576Glu
|
|
ENST00000425368.6:c.1728C>A
|
ENSP00000416561.2:p.Asp576Glu
|
|
ENST00000456570.5:c.3234C>A
|
ENSP00000410815.1:p.Asp1078Glu
|
|
ENST00000467360.1:n.854C>A
|
|
|
ENST00000477310.1:c.2781C>A
|
ENSP00000418996.1:p.Asp927Glu
|
|
ENST00000483004.1:c.350C>A
|
|
|
NM_001710.5:c.1728C>A , LRG_136t1:c.1728C>A
|
NP_001701.2:p.Asp576Glu
|
|
NM_001710.6:c.1728C>A
MANE Select
|
NP_001701.2:p.Asp576Glu
|
|