ENST00000395796.8:c.*947C>G
|
ENSP00000379142.4:n.*947C>G
|
|
ENST00000616242.5:c.*69C>G
|
ENSP00000482149.2:n.*69C>G
|
|
ENST00000683378.1:n.175C>G
|
|
|
ENST00000345378.7:c.952C>G
|
ENSP00000223366.2:p.His318Asp
|
|
ENST00000403799.8:c.949C>G
MANE Select
|
ENSP00000384247.3:p.His317Asp
|
|
ENST00000671824.1:c.1012C>G
|
ENSP00000500264.1:p.His338Asp
|
|
ENST00000673284.1:c.949C>G
|
ENSP00000499852.1:p.His317Asp
|
|
ENST00000345378.6:c.952C>G
|
ENSP00000223366.2:p.His318Asp
|
|
ENST00000395796.7:c.946C>G
|
ENSP00000379142.3:p.His316Asp
|
|
ENST00000403799.7:c.949C>G
|
ENSP00000384247.3:p.His317Asp
|
|
ENST00000437084.1:c.898C>G
|
ENSP00000402840.1:p.His300Asp
|
|
ENST00000473353.1:n.247C>G
|
|
|
ENST00000616242.4:c.946C>G
|
ENSP00000482149.1:p.His316Asp
|
|
NM_000162.3:c.949C>G
|
NP_000153.1:p.His317Asp
|
|
NM_033507.1:c.952C>G
|
NP_277042.1:p.His318Asp
|
|
NM_033508.1:c.946C>G
|
NP_277043.1:p.His316Asp
|
|
NM_000162.4:c.949C>G
|
NP_000153.1:p.His317Asp
|
|
NM_001354800.1:c.949C>G
|
NP_001341729.1:p.His317Asp
|
|
NM_001354801.1:c.8+86C>G
|
NP_001341730.1:n.8+86C>G
|
|
NM_033507.2:c.952C>G
|
NP_277042.1:p.His318Asp
|
|
NM_033508.2:c.946C>G
|
NP_277043.1:p.His316Asp
|
|
NM_000162.5:c.949C>G
MANE Select
|
NP_000153.1:p.His317Asp
|
|
NM_033507.3:c.952C>G
|
NP_277042.1:p.His318Asp
|
|
NM_033508.3:c.946C>G
|
NP_277043.1:p.His316Asp
|
|