ENST00000452035.7:n.2041T>G
|
|
|
ENST00000483004.2:c.1433T>G
|
ENSP00000419887.2:p.Ile478Arg
|
|
ENST00000698628.1:c.1624+240T>G
|
ENSP00000513848.1:n.1624+240T>G
|
|
ENST00000698629.1:n.1826T>G
|
|
|
ENST00000698630.1:n.2365T>G
|
|
|
ENST00000698631.1:n.2366T>G
|
|
|
ENST00000698632.1:n.3160T>G
|
|
|
ENST00000698633.1:n.3050T>G
|
|
|
ENST00000698636.1:n.1871T>G
|
|
|
ENST00000425368.7:c.1649T>G
MANE Select
|
ENSP00000416561.2:p.Ile550Arg
|
|
ENST00000425368.6:c.1649T>G
|
ENSP00000416561.2:p.Ile550Arg
|
|
ENST00000452035.6:n.1864T>G
|
|
|
ENST00000456570.5:c.3155T>G
|
ENSP00000410815.1:p.Ile1052Arg
|
|
ENST00000467360.1:n.775T>G
|
|
|
ENST00000477310.1:c.2702T>G
|
ENSP00000418996.1:p.Ile901Arg
|
|
ENST00000483004.1:c.271T>G
|
|
|
NM_001710.5:c.1649T>G , LRG_136t1:c.1649T>G
|
NP_001701.2:p.Ile550Arg
|
|
NM_001710.6:c.1649T>G
MANE Select
|
NP_001701.2:p.Ile550Arg
|
|