ENST00000682568.1:n.1816C>A
|
|
|
ENST00000682617.1:c.1876C>A
|
ENSP00000507912.1:p.Leu626Ile
|
|
ENST00000682826.1:c.*1052C>A
|
ENSP00000507274.1:n.*1052C>A
|
|
ENST00000682909.1:n.3778C>A
|
|
|
ENST00000683277.1:n.3383C>A
|
|
|
ENST00000683407.1:n.1746C>A
|
|
|
ENST00000683962.1:c.*1432C>A
|
ENSP00000506854.1:n.*1432C>A
|
|
ENST00000311895.8:c.1738C>A
MANE Select
|
ENSP00000310520.7:p.Leu580Ile
|
|
ENST00000311895.7:c.1738C>A
|
ENSP00000310520.7:p.Leu580Ile
|
|
ENST00000389138.7:n.1015C>A
|
|
|
NM_005236.2:c.1738C>A , LRG_463t1:c.1738C>A
|
NP_005227.1:p.Leu580Ile
|
|
XM_011522424.1:c.1876C>A
|
XP_011520726.1:p.Leu626Ile
|
|
XM_011522425.1:c.1195C>A
|
XP_011520727.1:p.Leu399Ile
|
|
XM_011522426.1:c.949C>A
|
XP_011520728.1:p.Leu317Ile
|
|
XM_011522427.1:c.388C>A
|
XP_011520729.1:p.Leu130Ile
|
|
XR_932805.1:n.1897C>A
|
|
|
XM_011522424.3:c.1876C>A
|
XP_011520726.1:p.Leu626Ile
|
|
XM_017023043.2:c.949C>A
|
XP_016878532.1:p.Leu317Ile
|
|
NM_005236.3:c.1738C>A
MANE Select
|
NP_005227.1:p.Leu580Ile
|
|