ENST00000452035.7:n.2138C>A
|
|
|
ENST00000483004.2:c.1530C>A
|
ENSP00000419887.2:p.Leu510=
|
|
ENST00000698628.1:c.1624+337C>A
|
ENSP00000513848.1:n.1624+337C>A
|
|
ENST00000698629.1:n.1923C>A
|
|
|
ENST00000698630.1:n.2462C>A
|
|
|
ENST00000698631.1:n.2463C>A
|
|
|
ENST00000698632.1:n.3257C>A
|
|
|
ENST00000698633.1:n.3147C>A
|
|
|
ENST00000698636.1:n.1968C>A
|
|
|
ENST00000425368.7:c.1746C>A
MANE Select
|
ENSP00000416561.2:p.Leu582=
|
|
ENST00000425368.6:c.1746C>A
|
ENSP00000416561.2:p.Leu582=
|
|
ENST00000456570.5:c.3252C>A
|
ENSP00000410815.1:p.Leu1084=
|
|
ENST00000467360.1:n.872C>A
|
|
|
ENST00000477310.1:c.2799C>A
|
ENSP00000418996.1:p.Leu933=
|
|
ENST00000483004.1:c.368C>A
|
|
|
NM_001710.5:c.1746C>A , LRG_136t1:c.1746C>A
|
NP_001701.2:p.Leu582=
|
|
NM_001710.6:c.1746C>A
MANE Select
|
NP_001701.2:p.Leu582=
|
|