ENST00000283871.10:c.273T>A
MANE Select
|
ENSP00000283871.5:p.Asp91Glu
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|
ENST00000283871.9:c.273T>A
|
ENSP00000283871.5:p.Asp91Glu
|
|
ENST00000466528.5:n.299T>A
|
|
|
ENST00000476082.2:c.150T>A
|
ENSP00000419560.2:p.Asp50Glu
|
|
ENST00000485313.5:n.381T>A
|
|
|
ENST00000488183.5:n.531T>A
|
|
|
NM_000187.3:c.273T>A
|
NP_000178.2:p.Asp91Glu
|
|
XM_005247412.1:c.273T>A
|
XP_005247469.1:p.Asp91Glu
|
|
XM_005247413.1:c.273T>A
|
XP_005247470.1:p.Asp91Glu
|
|
XM_005247414.3:c.273T>A
|
XP_005247471.1:p.Asp91Glu
|
|
XM_011512746.1:c.273T>A
|
XP_011511048.1:p.Asp91Glu
|
|
XM_005247412.2:c.273T>A
|
XP_005247469.1:p.Asp91Glu
|
|
XM_005247413.2:c.273T>A
|
XP_005247470.1:p.Asp91Glu
|
|
XM_005247414.5:c.273T>A
|
XP_005247471.1:p.Asp91Glu
|
|
XM_011512746.2:c.273T>A
|
XP_011511048.1:p.Asp91Glu
|
|
XM_017006277.2:c.-151T>A
|
XP_016861766.1:n.-151T>A
|
|
NM_000187.4:c.273T>A
MANE Select
|
NP_000178.2:p.Asp91Glu
|
|