ENST00000682568.1:n.1779A>G
|
|
|
ENST00000682617.1:c.1839A>G
|
ENSP00000507912.1:p.Thr613=
|
|
ENST00000682826.1:c.*1015A>G
|
ENSP00000507274.1:n.*1015A>G
|
|
ENST00000682909.1:n.3741A>G
|
|
|
ENST00000683277.1:n.3346A>G
|
|
|
ENST00000683407.1:n.1709A>G
|
|
|
ENST00000683962.1:c.*1395A>G
|
ENSP00000506854.1:n.*1395A>G
|
|
ENST00000311895.8:c.1701A>G
MANE Select
|
ENSP00000310520.7:p.Thr567=
|
|
ENST00000311895.7:c.1701A>G
|
ENSP00000310520.7:p.Thr567=
|
|
ENST00000389138.7:n.978A>G
|
|
|
NM_005236.2:c.1701A>G , LRG_463t1:c.1701A>G
|
NP_005227.1:p.Thr567=
|
|
XM_011522424.1:c.1839A>G
|
XP_011520726.1:p.Thr613=
|
|
XM_011522425.1:c.1158A>G
|
XP_011520727.1:p.Thr386=
|
|
XM_011522426.1:c.912A>G
|
XP_011520728.1:p.Thr304=
|
|
XM_011522427.1:c.351A>G
|
XP_011520729.1:p.Thr117=
|
|
XR_932805.1:n.1860A>G
|
|
|
XM_011522424.3:c.1839A>G
|
XP_011520726.1:p.Thr613=
|
|
XM_017023043.2:c.912A>G
|
XP_016878532.1:p.Thr304=
|
|
NM_005236.3:c.1701A>G
MANE Select
|
NP_005227.1:p.Thr567=
|
|