ENST00000298139.7:c.576C>G
MANE Select
|
ENSP00000298139.5:p.Asp192Glu
|
|
ENST00000650667.1:c.*190C>G
|
ENSP00000498593.1:n.*190C>G
|
|
ENST00000298139.5:c.576C>G
|
ENSP00000298139.5:p.Asp192Glu
|
|
NM_000553.4:c.576C>G , LRG_524t1:c.576C>G
|
NP_000544.2:p.Asp192Glu
|
|
XM_011544639.1:c.576C>G
|
XP_011542941.1:p.Asp192Glu
|
|
XR_949470.1:n.849C>G
|
|
|
XR_949471.1:n.849C>G
|
|
|
XR_949472.1:n.849C>G
|
|
|
NM_000553.5:c.576C>G
|
NP_000544.2:p.Asp192Glu
|
|
XM_011544639.3:c.576C>G
|
XP_011542941.1:p.Asp192Glu
|
|
XM_024447265.1:c.366C>G
|
XP_024303033.1:p.Asp122Glu
|
|
XR_949470.3:n.877C>G
|
|
|
XR_949471.3:n.877C>G
|
|
|
XR_949472.3:n.877C>G
|
|
|
NM_000553.6:c.576C>G
MANE Select
|
NP_000544.2:p.Asp192Glu
|
|