ENST00000246337.9:c.999C=
MANE Select
|
ENSP00000246337.4:p.Tyr333=
|
|
ENST00000491773.6:c.756C=
|
ENSP00000498551.1:p.Tyr252=
|
|
ENST00000636293.1:c.861C=
|
ENSP00000490710.1:p.Tyr287=
|
|
ENST00000636836.1:c.*35C=
|
ENSP00000490594.1:n.*35C=
|
|
ENST00000651476.1:c.894C=
|
ENSP00000498668.1:p.Tyr298=
|
|
ENST00000652165.1:c.756C=
|
ENSP00000498295.1:p.Tyr252=
|
|
ENST00000652287.1:c.936C=
|
ENSP00000498413.1:p.Tyr312=
|
|
ENST00000652514.1:c.960C=
|
ENSP00000498635.1:n.960C=
|
|
ENST00000246337.8:c.999C=
|
ENSP00000246337.4:p.Tyr333=
|
|
ENST00000465678.1:n.744C=
|
|
|
ENST00000472254.1:n.752C=
|
|
|
ENST00000494399.5:n.1666C=
|
|
|
NM_000374.4:c.999C=
|
NP_000365.3:p.Tyr333=
|
|
NR_036510.1:n.1182C=
|
|
|
XM_005271169.1:c.783C=
|
XP_005271226.1:p.Tyr261=
|
|
XM_005271170.1:c.783C=
|
XP_005271227.1:p.Tyr261=
|
|
XM_011542080.1:c.936C=
|
XP_011540382.1:p.Tyr312=
|
|
XM_011542081.1:c.831C=
|
XP_011540383.1:p.Tyr277=
|
|
NM_000374.5:c.999C=
MANE Select
|
NP_000365.3:p.Tyr333=
|
|
NR_158184.1:n.1080C=
|
|
|
NR_158185.1:n.1030C=
|
|
|
NR_036510.2:n.1061C=
|
|
|