ENST00000682568.1:n.1812G>T
|
|
|
ENST00000682617.1:c.1872G>T
|
ENSP00000507912.1:p.Val624=
|
|
ENST00000682826.1:c.*1048G>T
|
ENSP00000507274.1:n.*1048G>T
|
|
ENST00000682909.1:n.3774G>T
|
|
|
ENST00000683277.1:n.3379G>T
|
|
|
ENST00000683407.1:n.1742G>T
|
|
|
ENST00000683962.1:c.*1428G>T
|
ENSP00000506854.1:n.*1428G>T
|
|
ENST00000311895.8:c.1734G>T
MANE Select
|
ENSP00000310520.7:p.Val578=
|
|
ENST00000311895.7:c.1734G>T
|
ENSP00000310520.7:p.Val578=
|
|
ENST00000389138.7:n.1011G>T
|
|
|
NM_005236.2:c.1734G>T , LRG_463t1:c.1734G>T
|
NP_005227.1:p.Val578=
|
|
XM_011522424.1:c.1872G>T
|
XP_011520726.1:p.Val624=
|
|
XM_011522425.1:c.1191G>T
|
XP_011520727.1:p.Val397=
|
|
XM_011522426.1:c.945G>T
|
XP_011520728.1:p.Val315=
|
|
XM_011522427.1:c.384G>T
|
XP_011520729.1:p.Val128=
|
|
XR_932805.1:n.1893G>T
|
|
|
XM_011522424.3:c.1872G>T
|
XP_011520726.1:p.Val624=
|
|
XM_017023043.2:c.945G>T
|
XP_016878532.1:p.Val315=
|
|
NM_005236.3:c.1734G>T
MANE Select
|
NP_005227.1:p.Val578=
|
|