ENST00000682568.1:n.1783G>A
|
|
|
ENST00000682617.1:c.1843G>A
|
ENSP00000507912.1:p.Val615Ile
|
|
ENST00000682826.1:c.*1019G>A
|
ENSP00000507274.1:n.*1019G>A
|
|
ENST00000682909.1:n.3745G>A
|
|
|
ENST00000683277.1:n.3350G>A
|
|
|
ENST00000683407.1:n.1713G>A
|
|
|
ENST00000683962.1:c.*1399G>A
|
ENSP00000506854.1:n.*1399G>A
|
|
ENST00000311895.8:c.1705G>A
MANE Select
|
ENSP00000310520.7:p.Val569Ile
|
|
ENST00000311895.7:c.1705G>A
|
ENSP00000310520.7:p.Val569Ile
|
|
ENST00000389138.7:n.982G>A
|
|
|
NM_005236.2:c.1705G>A , LRG_463t1:c.1705G>A
|
NP_005227.1:p.Val569Ile
|
|
XM_011522424.1:c.1843G>A
|
XP_011520726.1:p.Val615Ile
|
|
XM_011522425.1:c.1162G>A
|
XP_011520727.1:p.Val388Ile
|
|
XM_011522426.1:c.916G>A
|
XP_011520728.1:p.Val306Ile
|
|
XM_011522427.1:c.355G>A
|
XP_011520729.1:p.Val119Ile
|
|
XR_932805.1:n.1864G>A
|
|
|
XM_011522424.3:c.1843G>A
|
XP_011520726.1:p.Val615Ile
|
|
XM_017023043.2:c.916G>A
|
XP_016878532.1:p.Val306Ile
|
|
NM_005236.3:c.1705G>A
MANE Select
|
NP_005227.1:p.Val569Ile
|
|