ENST00000369702.5:c.2089G>C
MANE Select
|
ENSP00000358716.4:p.Glu697Gln
|
|
ENST00000533164.6:c.*1503G>C
|
ENSP00000434085.1:n.*1503G>C
|
|
ENST00000534200.2:n.3824G>C
|
|
|
ENST00000679381.1:n.2711G>C
|
|
|
ENST00000679498.1:n.3947G>C
|
|
|
ENST00000679576.1:c.2424G>C
|
ENSP00000506357.1:n.2424G>C
|
|
ENST00000679724.1:c.2089G>C
|
ENSP00000505857.1:p.Glu697Gln
|
|
ENST00000679774.1:n.3714G>C
|
|
|
ENST00000680038.1:n.3081G>C
|
|
|
ENST00000680317.1:n.2437G>C
|
|
|
ENST00000680383.1:c.*968G>C
|
ENSP00000505119.1:n.*968G>C
|
|
ENST00000680415.1:n.3420G>C
|
|
|
ENST00000680518.1:c.*815G>C
|
ENSP00000506543.1:n.*815G>C
|
|
ENST00000680627.1:c.2089G>C
|
ENSP00000505758.1:p.Glu697Gln
|
|
ENST00000680936.1:c.*1317G>C
|
ENSP00000506651.1:n.*1317G>C
|
|
ENST00000680983.1:n.1958G>C
|
|
|
ENST00000681529.1:n.2811G>C
|
|
|
ENST00000681559.1:c.*1266G>C
|
ENSP00000506100.1:n.*1266G>C
|
|
ENST00000681747.1:n.3089G>C
|
|
|
ENST00000369702.4:c.2089G>C
|
ENSP00000358716.4:p.Glu697Gln
|
|
ENST00000475700.1:c.913G>C
|
ENSP00000435660.1:p.Glu305Gln
|
|
NM_007204.4:c.2089G>C
|
NP_009135.4:p.Glu697Gln
|
|
NM_007204.5:c.2089G>C
MANE Select
|
NP_009135.4:p.Glu697Gln
|
|