ENST00000682568.1:n.1877G>T
|
|
|
ENST00000682617.1:c.1937G>T
|
ENSP00000507912.1:p.Gly646Val
|
|
ENST00000682826.1:c.*1113G>T
|
ENSP00000507274.1:n.*1113G>T
|
|
ENST00000682909.1:n.3839G>T
|
|
|
ENST00000683277.1:n.3444G>T
|
|
|
ENST00000683407.1:n.1807G>T
|
|
|
ENST00000683962.1:c.*1493G>T
|
ENSP00000506854.1:n.*1493G>T
|
|
ENST00000311895.8:c.1799G>T
MANE Select
|
ENSP00000310520.7:p.Gly600Val
|
|
ENST00000311895.7:c.1799G>T
|
ENSP00000310520.7:p.Gly600Val
|
|
ENST00000389138.7:n.1076G>T
|
|
|
NM_005236.2:c.1799G>T , LRG_463t1:c.1799G>T
|
NP_005227.1:p.Gly600Val
|
|
XM_011522424.1:c.1937G>T
|
XP_011520726.1:p.Gly646Val
|
|
XM_011522425.1:c.1256G>T
|
XP_011520727.1:p.Gly419Val
|
|
XM_011522426.1:c.1010G>T
|
XP_011520728.1:p.Gly337Val
|
|
XM_011522427.1:c.449G>T
|
XP_011520729.1:p.Gly150Val
|
|
XR_932805.1:n.1958G>T
|
|
|
XM_011522424.3:c.1937G>T
|
XP_011520726.1:p.Gly646Val
|
|
XM_017023043.2:c.1010G>T
|
XP_016878532.1:p.Gly337Val
|
|
NM_005236.3:c.1799G>T
MANE Select
|
NP_005227.1:p.Gly600Val
|
|