ENST00000296589.9:c.566T>A
MANE Select
|
ENSP00000296589.4:p.Phe189Tyr
|
|
ENST00000296589.8:c.566T>A
|
ENSP00000296589.4:p.Phe189Tyr
|
|
ENST00000382102.7:c.566T>A
|
ENSP00000371534.3:p.Phe189Tyr
|
|
ENST00000505056.1:n.368T>A
|
|
|
ENST00000509381.1:c.563-9509T>A
|
ENSP00000421100.1:n.563-9509T>A
|
|
ENST00000510600.1:c.41T>A
|
ENSP00000424010.1:p.Phe14Tyr
|
|
NM_001012509.3:c.566T>A
|
NP_001012527.1:p.Phe189Tyr
|
|
NM_001297417.2:c.563-9509T>A
|
NP_001284346.2:n.563-9509T>A
|
|
NM_016180.4:c.566T>A
|
NP_057264.3:p.Phe189Tyr
|
|
XM_011514051.1:c.164T>A
|
XP_011512353.1:p.Phe55Tyr
|
|
XM_011514052.1:c.566T>A
|
XP_011512354.1:p.Phe189Tyr
|
|
XR_925620.1:n.1383T>A
|
|
|
NM_016180.5:c.566T>A
MANE Select
|
NP_057264.4:p.Phe189Tyr
|
|
NM_001012509.4:c.566T>A
|
NP_001012527.2:p.Phe189Tyr
|
|
NM_001297417.3:c.563-9509T>A
|
NP_001284346.2:n.563-9509T>A
|
|
NM_001297417.4:c.563-9509T>A
|
NP_001284346.2:n.563-9509T>A
|
|