ENST00000522719.4:c.475G=
(NKX2-1)
|
ENSP00000429519.4:p.Ala159=
|
|
ENST00000354822.7:c.565G=
(NKX2-1)
MANE Select
|
ENSP00000346879.6:p.Ala189=
|
|
ENST00000521945.1:n.54+1549G=
|
|
|
ENST00000522719.3:c.*602G=
(NKX2-1)
|
ENSP00000429519.3:n.*602G=
|
|
ENST00000546983.2:c.373+1066G=
|
ENSP00000449302.2:n.373+1066G=
|
|
ENST00000354822.6:c.565G=
(NKX2-1)
|
ENSP00000346879.5:p.Ala189=
|
|
ENST00000498187.6:c.475G=
(NKX2-1)
|
ENSP00000429607.2:p.Ala159=
|
|
ENST00000518149.5:c.475G=
(NKX2-1)
|
ENSP00000428341.1:p.Ala159=
|
|
ENST00000522719.2:c.475G=
(NKX2-1)
|
ENSP00000429519.2:p.Ala159=
|
|
NM_001079668.2:c.565G=
(NKX2-1)
|
NP_001073136.1:p.Ala189=
|
|
NM_003317.3:c.475G=
(NKX2-1)
|
NP_003308.1:p.Ala159=
|
|
NM_001352986.1:c.-283+1549G=
(SFTA3)
|
NP_001339915.1:n.-283+1549G=
|
|
NM_001352987.1:c.-237+1549G=
(SFTA3)
|
NP_001339916.1:n.-237+1549G=
|
|
NM_001079668.3:c.565G=
(NKX2-1)
MANE Select
|
NP_001073136.1:p.Ala189=
|
|
NM_003317.4:c.475G=
(NKX2-1)
|
NP_003308.1:p.Ala159=
|
|
NR_161364.1:n.89+1549G=
(SFTA3)
|
|
|
NR_161365.1:n.89+1549G=
(SFTA3)
|
|
|