ENST00000244020.5:c.867A>T
MANE Select
|
ENSP00000244020.3:p.Ile289=
|
|
ENST00000657241.1:c.654+297A>T
|
|
|
ENST00000662078.1:c.674+297A>T
|
ENSP00000499666.1:n.674+297A>T
|
|
ENST00000668808.1:c.824+43A>T
|
ENSP00000499517.1:n.824+43A>T
|
|
ENST00000670741.1:c.674+297A>T
|
ENSP00000499492.1:n.674+297A>T
|
|
ENST00000671022.1:n.957A>T
|
|
|
ENST00000244020.4:c.867A>T
|
ENSP00000244020.3:p.Ile289=
|
|
ENST00000483871.6:c.*727A>T
|
ENSP00000433544.1:n.*727A>T
|
|
NM_006275.5:c.867A>T
|
NP_006266.2:p.Ile289=
|
|
NR_034009.1:n.1305A>T
|
|
|
XR_936608.2:n.1626A>T
|
|
|
NM_006275.6:c.867A>T
MANE Select
|
NP_006266.2:p.Ile289=
|
|
NR_034009.2:n.1273A>T
|
|
|