ENST00000682617.1:c.2375T>A
|
ENSP00000507912.1:p.Ile792Asn
|
|
ENST00000683962.1:c.*1931T>A
|
ENSP00000506854.1:n.*1931T>A
|
|
ENST00000311895.8:c.2237T>A
MANE Select
|
ENSP00000310520.7:p.Ile746Asn
|
|
ENST00000311895.7:c.2237T>A
|
ENSP00000310520.7:p.Ile746Asn
|
|
ENST00000389138.7:n.1514T>A
|
|
|
ENST00000462862.1:c.550T>A
|
ENSP00000461322.1:n.550T>A
|
|
NM_005236.2:c.2237T>A , LRG_463t1:c.2237T>A
|
NP_005227.1:p.Ile746Asn
|
|
XM_011522424.1:c.2375T>A
|
XP_011520726.1:p.Ile792Asn
|
|
XM_011522425.1:c.1694T>A
|
XP_011520727.1:p.Ile565Asn
|
|
XM_011522426.1:c.1448T>A
|
XP_011520728.1:p.Ile483Asn
|
|
XM_011522427.1:c.887T>A
|
XP_011520729.1:p.Ile296Asn
|
|
XR_932805.1:n.2396T>A
|
|
|
XM_011522424.3:c.2375T>A
|
XP_011520726.1:p.Ile792Asn
|
|
XM_017023043.2:c.1448T>A
|
XP_016878532.1:p.Ile483Asn
|
|
NM_005236.3:c.2237T>A
MANE Select
|
NP_005227.1:p.Ile746Asn
|
|