ENST00000261978.9:c.5408A>G
MANE Select
|
ENSP00000261978.4:p.His1803Arg
|
|
ENST00000261978.8:c.5408A>G
|
ENSP00000261978.4:p.His1803Arg
|
|
ENST00000553939.5:c.*187A>G
|
ENSP00000452110.1:n.*187A>G
|
|
ENST00000554861.1:n.626A>G
|
|
|
ENST00000556690.5:c.5276A>G
|
ENSP00000451477.1:p.His1759Arg
|
|
NM_000428.2:c.5408A>G
|
NP_000419.1:p.His1803Arg
|
|
XM_011536765.1:c.5027A>G
|
XP_011535067.1:p.His1676Arg
|
|
XM_011536766.1:c.4949A>G
|
XP_011535068.1:p.His1650Arg
|
|
XM_011536767.1:c.4925A>G
|
XP_011535069.1:p.His1642Arg
|
|
XM_011536765.2:c.5027A>G
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XP_011535067.1:p.His1676Arg
|
|
NM_000428.3:c.5408A>G
MANE Select
|
NP_000419.1:p.His1803Arg
|
|