ENST00000452035.7:n.2059A>C
|
|
|
ENST00000483004.2:c.1451A>C
|
ENSP00000419887.2:p.His484Pro
|
|
ENST00000698628.1:c.1624+258A>C
|
ENSP00000513848.1:n.1624+258A>C
|
|
ENST00000698629.1:n.1844A>C
|
|
|
ENST00000698630.1:n.2383A>C
|
|
|
ENST00000698631.1:n.2384A>C
|
|
|
ENST00000698632.1:n.3178A>C
|
|
|
ENST00000698633.1:n.3068A>C
|
|
|
ENST00000698636.1:n.1889A>C
|
|
|
ENST00000425368.7:c.1667A>C
MANE Select
|
ENSP00000416561.2:p.His556Pro
|
|
ENST00000425368.6:c.1667A>C
|
ENSP00000416561.2:p.His556Pro
|
|
ENST00000456570.5:c.3173A>C
|
ENSP00000410815.1:p.His1058Pro
|
|
ENST00000467360.1:n.793A>C
|
|
|
ENST00000477310.1:c.2720A>C
|
ENSP00000418996.1:p.His907Pro
|
|
ENST00000483004.1:c.289A>C
|
|
|
NM_001710.5:c.1667A>C , LRG_136t1:c.1667A>C
|
NP_001701.2:p.His556Pro
|
|
NM_001710.6:c.1667A>C
MANE Select
|
NP_001701.2:p.His556Pro
|
|