|
ENST00000700029.2:c.385G>C
|
ENSP00000514759.2:p.Gly129Arg
|
|
|
ENST00000710265.1:c.385G>C
|
ENSP00000518161.1:p.Gly129Arg
|
|
|
ENST00000472832.3:c.385G>C
|
ENSP00000483066.2:p.Gly129Arg
|
|
|
ENST00000688158.2:n.1120G>C
|
|
|
|
ENST00000688922.2:c.*215G>C
|
ENSP00000508742.2:n.*215G>C
|
|
|
ENST00000700021.1:c.340G>C
|
ENSP00000514757.1:p.Gly114Arg
|
|
|
ENST00000700022.1:c.385G>C
|
ENSP00000514758.1:p.Gly129Arg
|
|
|
ENST00000700029.1:c.219G>C
|
|
|
|
ENST00000706954.1:c.385G>C
|
ENSP00000516674.1:p.Gly129Arg
|
|
|
ENST00000706955.1:c.*420G>C
|
ENSP00000516675.1:n.*420G>C
|
|
|
ENST00000686459.1:c.385G>C
|
ENSP00000508909.1:p.Gly129Arg
|
|
|
ENST00000688158.1:c.*496G>C
|
ENSP00000509254.1:n.*496G>C
|
|
|
ENST00000688308.1:c.385G>C
|
ENSP00000508752.1:p.Gly129Arg
|
|
|
ENST00000688922.1:c.306G>C
|
|
|
|
ENST00000693560.1:c.904G>C
|
ENSP00000509861.1:p.Gly302Arg
|
|
|
ENST00000371953.8:c.385G>C
MANE Select
|
ENSP00000361021.3:p.Gly129Arg
|
|
|
ENST00000371953.7:c.385G>C
|
ENSP00000361021.3:p.Gly129Arg
|
|
|
ENST00000498703.1:n.211G>C
|
|
|
|
ENST00000610634.1:c.283G>C
|
ENSP00000477517.1:p.Gly95Arg
|
|
|
NM_000314.5:c.385G>C
|
NP_000305.3:p.Gly129Arg
|
|
|
NM_000314.6:c.385G>C
|
NP_000305.3:p.Gly129Arg
|
|
|
NM_001304717.2:c.904G>C
|
NP_001291646.2:p.Gly302Arg
|
|
|
NM_001304718.1:c.-366G>C
|
NP_001291647.1:n.-366G>C
|
|
|
XM_006717926.2:c.340G>C
|
XP_006717989.1:p.Gly114Arg
|
|
|
XM_011539981.1:c.385G>C
|
XP_011538283.1:p.Gly129Arg
|
|
|
XM_011539982.1:c.289G>C
|
XP_011538284.1:p.Gly97Arg
|
|
|
XR_945789.1:n.1097G>C
|
|
|
|
XR_945790.1:n.1097G>C
|
|
|
|
XR_945791.1:n.1097G>C
|
|
|
|
NM_000314.7:c.385G>C
|
NP_000305.3:p.Gly129Arg
|
|
|
NM_001304717.5:c.904G>C
|
NP_001291646.4:p.Gly302Arg
|
|
|
NM_001304718.2:c.-366G>C
|
NP_001291647.1:n.-366G>C
|
|
|
NM_000314.8:c.385G>C
MANE Select
|
NP_000305.3:p.Gly129Arg
|
|
