ENST00000369762.7:c.974T>A
MANE Select
|
ENSP00000358777.2:p.Phe325Tyr
|
|
ENST00000439372.6:c.*936T>A
|
ENSP00000408317.1:n.*936T>A
|
|
ENST00000484908.2:n.1500T>A
|
|
|
ENST00000619046.5:c.590T>A
|
ENSP00000482243.2:p.Phe197Tyr
|
|
ENST00000677332.1:c.909T>A
|
ENSP00000502914.1:n.909T>A
|
|
ENST00000677342.1:c.*252T>A
|
ENSP00000503173.1:n.*252T>A
|
|
ENST00000678317.1:n.1506T>A
|
|
|
ENST00000679241.1:c.*40T>A
|
ENSP00000503588.1:n.*40T>A
|
|
ENST00000369762.6:c.974T>A
|
ENSP00000358777.2:p.Phe325Tyr
|
|
ENST00000422890.5:c.716T>A
|
ENSP00000398511.1:p.Phe239Tyr
|
|
ENST00000429585.5:c.666T>A
|
ENSP00000408470.1:n.666T>A
|
|
ENST00000455205.5:c.3452T>A
|
|
|
ENST00000491569.5:n.1016T>A
|
|
|
ENST00000619046.4:c.407T>A
|
ENSP00000482243.1:p.Phe136Tyr
|
|
NM_001183.5:c.974T>A
|
NP_001174.2:p.Phe325Tyr
|
|
XM_011531179.1:c.407T>A
|
XP_011529481.1:p.Phe136Tyr
|
|
NM_001183.6:c.974T>A
MANE Select
|
NP_001174.2:p.Phe325Tyr
|
|