ENST00000246337.9:c.999C>G
MANE Select
|
ENSP00000246337.4:p.Tyr333Ter
|
|
ENST00000491773.6:c.756C>G
|
ENSP00000498551.1:p.Tyr252Ter
|
|
ENST00000636293.1:c.861C>G
|
ENSP00000490710.1:p.Tyr287Ter
|
|
ENST00000636836.1:c.*35C>G
|
ENSP00000490594.1:n.*35C>G
|
|
ENST00000651476.1:c.894C>G
|
ENSP00000498668.1:p.Tyr298Ter
|
|
ENST00000652165.1:c.756C>G
|
ENSP00000498295.1:p.Tyr252Ter
|
|
ENST00000652287.1:c.936C>G
|
ENSP00000498413.1:p.Tyr312Ter
|
|
ENST00000652514.1:c.960C>G
|
ENSP00000498635.1:n.960C>G
|
|
ENST00000246337.8:c.999C>G
|
ENSP00000246337.4:p.Tyr333Ter
|
|
ENST00000465678.1:n.744C>G
|
|
|
ENST00000472254.1:n.752C>G
|
|
|
ENST00000494399.5:n.1666C>G
|
|
|
NM_000374.4:c.999C>G
|
NP_000365.3:p.Tyr333Ter
|
|
NR_036510.1:n.1182C>G
|
|
|
XM_005271169.1:c.783C>G
|
XP_005271226.1:p.Tyr261Ter
|
|
XM_005271170.1:c.783C>G
|
XP_005271227.1:p.Tyr261Ter
|
|
XM_011542080.1:c.936C>G
|
XP_011540382.1:p.Tyr312Ter
|
|
XM_011542081.1:c.831C>G
|
XP_011540383.1:p.Tyr277Ter
|
|
NM_000374.5:c.999C>G
MANE Select
|
NP_000365.3:p.Tyr333Ter
|
|
NR_158184.1:n.1080C>G
|
|
|
NR_158185.1:n.1030C>G
|
|
|
NR_036510.2:n.1061C>G
|
|
|