ENST00000452035.7:n.2104A=
|
|
|
ENST00000483004.2:c.1496A=
|
ENSP00000419887.2:p.Glu499=
|
|
ENST00000698628.1:c.1624+303A=
|
ENSP00000513848.1:n.1624+303A=
|
|
ENST00000698629.1:n.1889A=
|
|
|
ENST00000698630.1:n.2428A=
|
|
|
ENST00000698631.1:n.2429A=
|
|
|
ENST00000698632.1:n.3223A=
|
|
|
ENST00000698633.1:n.3113A=
|
|
|
ENST00000698636.1:n.1934A=
|
|
|
ENST00000425368.7:c.1712A=
MANE Select
|
ENSP00000416561.2:p.Glu571=
|
|
ENST00000425368.6:c.1712A=
|
ENSP00000416561.2:p.Glu571=
|
|
ENST00000456570.5:c.3218A=
|
ENSP00000410815.1:p.Glu1073=
|
|
ENST00000467360.1:n.838A=
|
|
|
ENST00000477310.1:c.2765A=
|
ENSP00000418996.1:p.Glu922=
|
|
ENST00000483004.1:c.334A=
|
|
|
NM_001710.5:c.1712A= , LRG_136t1:c.1712A=
|
NP_001701.2:p.Glu571=
|
|
NM_001710.6:c.1712A=
MANE Select
|
NP_001701.2:p.Glu571=
|
|