ENST00000405460.9:c.10846G>C
MANE Select
|
ENSP00000384582.2:p.Glu3616Gln
|
|
ENST00000639431.1:c.265+69458G>C
|
ENSP00000491057.1:n.265+69458G>C
|
|
ENST00000640374.1:n.3990G>C
|
|
|
ENST00000640464.1:n.1265G>C
|
|
|
ENST00000405460.6:c.10846G>C
|
ENSP00000384582.2:p.Glu3616Gln
|
|
ENST00000509621.1:c.3543G>C
|
|
|
NM_032119.3:c.10846G>C
|
NP_115495.3:p.Glu3616Gln
|
|
NR_003149.1:n.10859G>C
|
|
|
XM_011543675.1:c.10843G>C
|
XP_011541977.1:p.Glu3615Gln
|
|
XM_011543676.1:c.10765G>C
|
XP_011541978.1:p.Glu3589Gln
|
|
XM_011543677.1:c.8149G>C
|
XP_011541979.1:p.Glu2717Gln
|
|
XM_011543678.1:c.10846G>C
|
XP_011541980.1:p.Glu3616Gln
|
|
XM_011543679.1:c.*68G>C
|
XP_011541981.1:n.*68G>C
|
|
NM_032119.4:c.10846G>C
MANE Select
|
NP_115495.3:p.Glu3616Gln
|
|
XM_017009963.2:c.10867G>C
|
XP_016865452.1:p.Glu3623Gln
|
|
XM_017009964.2:c.10864G>C
|
XP_016865453.1:p.Glu3622Gln
|
|
XM_017009965.1:c.10864G>C
|
XP_016865454.1:p.Glu3622Gln
|
|
XM_017009966.2:c.10786G>C
|
XP_016865455.1:p.Glu3596Gln
|
|
XM_017009967.1:c.10771G>C
|
XP_016865456.1:p.Glu3591Gln
|
|
XM_017009968.2:c.10867G>C
|
XP_016865457.1:p.Glu3623Gln
|
|
XM_017009969.2:c.10867G>C
|
XP_016865458.1:p.Glu3623Gln
|
|
XM_017009970.2:c.10867G>C
|
XP_016865459.1:p.Glu3623Gln
|
|
XM_017009971.2:c.10867G>C
|
XP_016865460.1:p.Glu3623Gln
|
|
XM_017009972.1:c.3985G>C
|
XP_016865461.1:p.Glu1329Gln
|
|
XM_017009973.1:c.3964G>C
|
XP_016865462.1:p.Glu1322Gln
|
|
XM_017009974.2:c.*68G>C
|
XP_016865463.1:n.*68G>C
|
|
NR_003149.2:n.10862G>C
|
|
|