ENST00000456935.7:c.593T>A
MANE Select
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ENSP00000395473.2:p.Phe198Tyr
|
|
ENST00000221363.8:c.593T>A
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ENSP00000221363.4:p.Phe198Tyr
|
|
ENST00000456935.6:c.593T>A
|
ENSP00000395473.2:p.Phe198Tyr
|
|
ENST00000466794.5:n.575T>A
|
|
|
ENST00000486847.2:c.333+523T>A
|
ENSP00000470174.1:n.333+523T>A
|
|
ENST00000596512.5:n.531T>A
|
|
|
ENST00000597961.1:c.584T>A
|
ENSP00000472710.1:p.Phe195Tyr
|
|
NM_000528.3:c.593T>A
|
NP_000519.2:p.Phe198Tyr
|
|
NM_001173498.1:c.593T>A
|
NP_001166969.1:p.Phe198Tyr
|
|
XM_005259913.1:c.593T>A
|
XP_005259970.1:p.Phe198Tyr
|
|
XM_005259913.2:c.593T>A
|
XP_005259970.1:p.Phe198Tyr
|
|
XM_024451518.1:c.-426T>A
|
XP_024307286.1:n.-426T>A
|
|
NM_000528.4:c.593T>A
MANE Select
|
NP_000519.2:p.Phe198Tyr
|
|
NM_001173498.2:c.593T>A
|
NP_001166969.1:p.Phe198Tyr
|
|