ENST00000539215.6:c.511G>C
|
|
|
ENST00000699982.1:c.1610G>C
|
|
|
ENST00000699983.1:c.1610G>C
|
|
|
ENST00000699984.1:c.1610G>C
|
|
|
ENST00000320574.10:c.1756G>C
MANE Select
|
ENSP00000322570.5:p.Glu586Gln
|
|
ENST00000672742.1:c.*1258G>C
|
ENSP00000500279.1:n.*1258G>C
|
|
ENST00000320574.9:c.1756G>C
|
ENSP00000322570.5:p.Glu586Gln
|
|
ENST00000535270.5:c.1675G>C
|
ENSP00000445753.1:p.Glu559Gln
|
|
ENST00000537064.5:c.*803G>C
|
ENSP00000442578.1:n.*803G>C
|
|
NM_006231.3:c.1756G>C , LRG_789t1:c.1756G>C
|
NP_006222.2:p.Glu586Gln
|
|
XM_011534795.1:c.1756G>C
|
XP_011533097.1:p.Glu586Gln
|
|
XM_011534796.1:c.1627G>C
|
XP_011533098.1:p.Glu543Gln
|
|
XM_011534797.1:c.835G>C
|
XP_011533099.1:p.Glu279Gln
|
|
XM_011534798.1:c.418G>C
|
XP_011533100.1:p.Glu140Gln
|
|
XM_011534799.1:c.1756G>C
|
XP_011533101.1:p.Glu586Gln
|
|
XM_011534800.1:c.1756G>C
|
XP_011533102.1:p.Glu586Gln
|
|
XM_011534801.1:c.1756G>C
|
XP_011533103.1:p.Glu586Gln
|
|
XR_941395.1:n.1965G>C
|
|
|
XM_011534795.3:c.1756G>C
|
XP_011533097.1:p.Glu586Gln
|
|
XM_011534797.3:c.835G>C
|
XP_011533099.1:p.Glu279Gln
|
|
XM_011534799.2:c.1756G>C
|
XP_011533101.1:p.Glu586Gln
|
|
XR_002957338.1:n.1960G>C
|
|
|
XR_002957339.1:n.1960G>C
|
|
|
XR_941395.2:n.1960G>C
|
|
|
NM_006231.4:c.1756G>C
MANE Select
|
NP_006222.2:p.Glu586Gln
|
|