ENST00000452035.7:n.2062C>A
|
|
|
ENST00000483004.2:c.1454C>A
|
ENSP00000419887.2:p.Pro485His
|
|
ENST00000698628.1:c.1624+261C>A
|
ENSP00000513848.1:n.1624+261C>A
|
|
ENST00000698629.1:n.1847C>A
|
|
|
ENST00000698630.1:n.2386C>A
|
|
|
ENST00000698631.1:n.2387C>A
|
|
|
ENST00000698632.1:n.3181C>A
|
|
|
ENST00000698633.1:n.3071C>A
|
|
|
ENST00000698636.1:n.1892C>A
|
|
|
ENST00000425368.7:c.1670C>A
MANE Select
|
ENSP00000416561.2:p.Pro557His
|
|
ENST00000425368.6:c.1670C>A
|
ENSP00000416561.2:p.Pro557His
|
|
ENST00000456570.5:c.3176C>A
|
ENSP00000410815.1:p.Pro1059His
|
|
ENST00000467360.1:n.796C>A
|
|
|
ENST00000477310.1:c.2723C>A
|
ENSP00000418996.1:p.Pro908His
|
|
ENST00000483004.1:c.292C>A
|
|
|
NM_001710.5:c.1670C>A , LRG_136t1:c.1670C>A
|
NP_001701.2:p.Pro557His
|
|
NM_001710.6:c.1670C>A
MANE Select
|
NP_001701.2:p.Pro557His
|
|