ENST00000261304.7:c.941A=
MANE Select
|
ENSP00000261304.2:p.Tyr314=
|
|
ENST00000261304.6:c.941A=
|
ENSP00000261304.2:p.Tyr314=
|
|
ENST00000393568.8:c.872A=
|
ENSP00000377198.4:p.Tyr291=
|
|
ENST00000393569.6:c.863A=
|
ENSP00000377199.2:p.Tyr288=
|
|
ENST00000474294.6:n.931A=
|
|
|
ENST00000544807.6:c.773A=
|
ENSP00000437513.2:p.Tyr258=
|
|
ENST00000555000.5:c.308A=
|
ENSP00000450472.1:p.Tyr103=
|
|
ENST00000557316.5:c.*339A=
|
ENSP00000452314.1:n.*339A=
|
|
ENST00000557520.1:n.27A=
|
|
|
ENST00000622264.4:c.931A=
|
|
|
NM_000153.3:c.941A=
|
NP_000144.2:p.Tyr314=
|
|
NM_001201401.1:c.872A=
|
NP_001188330.1:p.Tyr291=
|
|
NM_001201402.1:c.863A=
|
NP_001188331.1:p.Tyr288=
|
|
XM_011536618.1:c.773A=
|
XP_011534920.1:p.Tyr258=
|
|
XM_011536618.2:c.773A=
|
XP_011534920.1:p.Tyr258=
|
|
NM_000153.4:c.941A=
MANE Select
|
NP_000144.2:p.Tyr314=
|
|
NM_001201401.2:c.872A=
|
NP_001188330.1:p.Tyr291=
|
|
NM_001201402.2:c.863A=
|
NP_001188331.1:p.Tyr288=
|
|