ENST00000244020.5:c.656T>A
MANE Select
|
ENSP00000244020.3:p.Ile219Asn
|
|
ENST00000657241.1:c.636T>A
|
|
|
ENST00000662078.1:c.656T>A
|
ENSP00000499666.1:p.Ile219Asn
|
|
ENST00000668808.1:c.656T>A
|
ENSP00000499517.1:p.Ile219Asn
|
|
ENST00000670741.1:c.656T>A
|
ENSP00000499492.1:p.Ile219Asn
|
|
ENST00000671022.1:n.746T>A
|
|
|
ENST00000244020.4:c.656T>A
|
ENSP00000244020.3:p.Ile219Asn
|
|
ENST00000483871.6:c.*516T>A
|
ENSP00000433544.1:n.*516T>A
|
|
NM_006275.5:c.656T>A
|
NP_006266.2:p.Ile219Asn
|
|
NR_034009.1:n.1094T>A
|
|
|
XR_936608.1:n.1415T>A
|
|
|
XR_936608.2:n.1415T>A
|
|
|
NM_006275.6:c.656T>A
MANE Select
|
NP_006266.2:p.Ile219Asn
|
|
NR_034009.2:n.1062T>A
|
|
|