ENST00000682568.1:n.1754G>T
|
|
|
ENST00000682617.1:c.1814G>T
|
ENSP00000507912.1:p.Gly605Val
|
|
ENST00000682826.1:c.*990G>T
|
ENSP00000507274.1:n.*990G>T
|
|
ENST00000682909.1:n.3716G>T
|
|
|
ENST00000683277.1:n.3321G>T
|
|
|
ENST00000683407.1:n.1684G>T
|
|
|
ENST00000683962.1:c.*1370G>T
|
ENSP00000506854.1:n.*1370G>T
|
|
ENST00000311895.8:c.1676G>T
MANE Select
|
ENSP00000310520.7:p.Gly559Val
|
|
ENST00000311895.7:c.1676G>T
|
ENSP00000310520.7:p.Gly559Val
|
|
ENST00000389138.7:n.953G>T
|
|
|
NM_005236.2:c.1676G>T , LRG_463t1:c.1676G>T
|
NP_005227.1:p.Gly559Val
|
|
XM_011522424.1:c.1814G>T
|
XP_011520726.1:p.Gly605Val
|
|
XM_011522425.1:c.1133G>T
|
XP_011520727.1:p.Gly378Val
|
|
XM_011522426.1:c.887G>T
|
XP_011520728.1:p.Gly296Val
|
|
XM_011522427.1:c.326G>T
|
XP_011520729.1:p.Gly109Val
|
|
XR_932805.1:n.1835G>T
|
|
|
XM_011522424.3:c.1814G>T
|
XP_011520726.1:p.Gly605Val
|
|
XM_017023043.2:c.887G>T
|
XP_016878532.1:p.Gly296Val
|
|
NM_005236.3:c.1676G>T
MANE Select
|
NP_005227.1:p.Gly559Val
|
|