ENST00000261978.9:c.5409C>G
MANE Select
|
ENSP00000261978.4:p.His1803Gln
|
|
ENST00000261978.8:c.5409C>G
|
ENSP00000261978.4:p.His1803Gln
|
|
ENST00000553939.5:c.*188C>G
|
ENSP00000452110.1:n.*188C>G
|
|
ENST00000554861.1:n.627C>G
|
|
|
ENST00000556690.5:c.5277C>G
|
ENSP00000451477.1:p.His1759Gln
|
|
NM_000428.2:c.5409C>G
|
NP_000419.1:p.His1803Gln
|
|
XM_011536765.1:c.5028C>G
|
XP_011535067.1:p.His1676Gln
|
|
XM_011536766.1:c.4950C>G
|
XP_011535068.1:p.His1650Gln
|
|
XM_011536767.1:c.4926C>G
|
XP_011535069.1:p.His1642Gln
|
|
XM_011536765.2:c.5028C>G
|
XP_011535067.1:p.His1676Gln
|
|
NM_000428.3:c.5409C>G
MANE Select
|
NP_000419.1:p.His1803Gln
|
|