ENST00000682568.1:n.1842T>A
|
|
|
ENST00000682617.1:c.1902T>A
|
ENSP00000507912.1:p.Val634=
|
|
ENST00000682826.1:c.*1078T>A
|
ENSP00000507274.1:n.*1078T>A
|
|
ENST00000682909.1:n.3804T>A
|
|
|
ENST00000683277.1:n.3409T>A
|
|
|
ENST00000683407.1:n.1772T>A
|
|
|
ENST00000683962.1:c.*1458T>A
|
ENSP00000506854.1:n.*1458T>A
|
|
ENST00000311895.8:c.1764T>A
MANE Select
|
ENSP00000310520.7:p.Val588=
|
|
ENST00000311895.7:c.1764T>A
|
ENSP00000310520.7:p.Val588=
|
|
ENST00000389138.7:n.1041T>A
|
|
|
NM_005236.2:c.1764T>A , LRG_463t1:c.1764T>A
|
NP_005227.1:p.Val588=
|
|
XM_011522424.1:c.1902T>A
|
XP_011520726.1:p.Val634=
|
|
XM_011522425.1:c.1221T>A
|
XP_011520727.1:p.Val407=
|
|
XM_011522426.1:c.975T>A
|
XP_011520728.1:p.Val325=
|
|
XM_011522427.1:c.414T>A
|
XP_011520729.1:p.Val138=
|
|
XR_932805.1:n.1923T>A
|
|
|
XM_011522424.3:c.1902T>A
|
XP_011520726.1:p.Val634=
|
|
XM_017023043.2:c.975T>A
|
XP_016878532.1:p.Val325=
|
|
NM_005236.3:c.1764T>A
MANE Select
|
NP_005227.1:p.Val588=
|
|