ENST00000682568.1:n.1807T>A
|
|
|
ENST00000682617.1:c.1867T>A
|
ENSP00000507912.1:p.Tyr623Asn
|
|
ENST00000682826.1:c.*1043T>A
|
ENSP00000507274.1:n.*1043T>A
|
|
ENST00000682909.1:n.3769T>A
|
|
|
ENST00000683277.1:n.3374T>A
|
|
|
ENST00000683407.1:n.1737T>A
|
|
|
ENST00000683962.1:c.*1423T>A
|
ENSP00000506854.1:n.*1423T>A
|
|
ENST00000311895.8:c.1729T>A
MANE Select
|
ENSP00000310520.7:p.Tyr577Asn
|
|
ENST00000311895.7:c.1729T>A
|
ENSP00000310520.7:p.Tyr577Asn
|
|
ENST00000389138.7:n.1006T>A
|
|
|
NM_005236.2:c.1729T>A , LRG_463t1:c.1729T>A
|
NP_005227.1:p.Tyr577Asn
|
|
XM_011522424.1:c.1867T>A
|
XP_011520726.1:p.Tyr623Asn
|
|
XM_011522425.1:c.1186T>A
|
XP_011520727.1:p.Tyr396Asn
|
|
XM_011522426.1:c.940T>A
|
XP_011520728.1:p.Tyr314Asn
|
|
XM_011522427.1:c.379T>A
|
XP_011520729.1:p.Tyr127Asn
|
|
XR_932805.1:n.1888T>A
|
|
|
XM_011522424.3:c.1867T>A
|
XP_011520726.1:p.Tyr623Asn
|
|
XM_017023043.2:c.940T>A
|
XP_016878532.1:p.Tyr314Asn
|
|
NM_005236.3:c.1729T>A
MANE Select
|
NP_005227.1:p.Tyr577Asn
|
|