ENST00000682568.1:n.1557C>G
|
|
|
ENST00000682617.1:c.1617C>G
|
ENSP00000507912.1:p.Thr539=
|
|
ENST00000682826.1:c.*793C>G
|
ENSP00000507274.1:n.*793C>G
|
|
ENST00000682909.1:n.3519C>G
|
|
|
ENST00000683277.1:n.3124C>G
|
|
|
ENST00000683407.1:n.1487C>G
|
|
|
ENST00000683962.1:c.*1173C>G
|
ENSP00000506854.1:n.*1173C>G
|
|
ENST00000311895.8:c.1479C>G
MANE Select
|
ENSP00000310520.7:p.Thr493=
|
|
ENST00000311895.7:c.1479C>G
|
ENSP00000310520.7:p.Thr493=
|
|
ENST00000389138.7:n.756C>G
|
|
|
NM_005236.2:c.1479C>G , LRG_463t1:c.1479C>G
|
NP_005227.1:p.Thr493=
|
|
XM_011522424.1:c.1617C>G
|
XP_011520726.1:p.Thr539=
|
|
XM_011522425.1:c.936C>G
|
XP_011520727.1:p.Thr312=
|
|
XM_011522426.1:c.690C>G
|
XP_011520728.1:p.Thr230=
|
|
XM_011522427.1:c.129C>G
|
XP_011520729.1:p.Thr43=
|
|
XR_932805.1:n.1638C>G
|
|
|
XM_011522424.3:c.1617C>G
|
XP_011520726.1:p.Thr539=
|
|
XM_017023043.2:c.690C>G
|
XP_016878532.1:p.Thr230=
|
|
NM_005236.3:c.1479C>G
MANE Select
|
NP_005227.1:p.Thr493=
|
|