ENST00000452035.7:n.2120C>T
|
|
|
ENST00000483004.2:c.1512C>T
|
ENSP00000419887.2:p.Asp504=
|
|
ENST00000698628.1:c.1624+319C>T
|
ENSP00000513848.1:n.1624+319C>T
|
|
ENST00000698629.1:n.1905C>T
|
|
|
ENST00000698630.1:n.2444C>T
|
|
|
ENST00000698631.1:n.2445C>T
|
|
|
ENST00000698632.1:n.3239C>T
|
|
|
ENST00000698633.1:n.3129C>T
|
|
|
ENST00000698636.1:n.1950C>T
|
|
|
ENST00000425368.7:c.1728C>T
MANE Select
|
ENSP00000416561.2:p.Asp576=
|
|
ENST00000425368.6:c.1728C>T
|
ENSP00000416561.2:p.Asp576=
|
|
ENST00000456570.5:c.3234C>T
|
ENSP00000410815.1:p.Asp1078=
|
|
ENST00000467360.1:n.854C>T
|
|
|
ENST00000477310.1:c.2781C>T
|
ENSP00000418996.1:p.Asp927=
|
|
ENST00000483004.1:c.350C>T
|
|
|
NM_001710.5:c.1728C>T , LRG_136t1:c.1728C>T
|
NP_001701.2:p.Asp576=
|
|
NM_001710.6:c.1728C>T
MANE Select
|
NP_001701.2:p.Asp576=
|
|