ENST00000220058.9:c.200A>G
MANE Select
|
ENSP00000220058.4:p.His67Arg
|
|
ENST00000220058.8:c.200A>G
|
ENSP00000220058.4:p.His67Arg
|
|
ENST00000543678.1:c.200A>G
|
ENSP00000443754.1:p.His67Arg
|
|
ENST00000558460.5:c.200A>G
|
ENSP00000452646.1:p.His67Arg
|
|
ENST00000558614.1:n.161A>G
|
|
|
ENST00000559633.1:n.119A>G
|
|
|
ENST00000560717.5:c.185A>G
|
ENSP00000457257.1:p.His62Arg
|
|
NM_139242.3:c.200A>G
|
NP_640335.2:p.His67Arg
|
|
XM_005254158.5:c.200A>G
|
XP_005254215.2:p.His67Arg
|
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XR_001751081.1:n.215A>G
|
|
|
NM_139242.4:c.200A>G
MANE Select
|
NP_640335.2:p.His67Arg
|
|