|
NM_032119.4:c.16010G>A
MANE Select
|
NP_115495.3:p.Gly5337Glu
|
|
ENST00000405460.9:c.16010G>A
MANE Select
|
ENSP00000384582.2:p.Gly5337Glu
|
|
NM_032119.3:c.16010G>A
|
NP_115495.3:p.Gly5337Glu
|
|
NR_003149.1:n.16023G>A
|
|
|
NR_003149.2:n.16026G>A
|
|
|
ENST00000405460.6:c.16010G>A
|
ENSP00000384582.2:p.Gly5337Glu
|
|
ENST00000425867.2:c.2993G>A
|
ENSP00000392618.2:p.Gly998Glu
|
|
ENST00000425867.3:c.4964G>A
|
ENSP00000392618.3:p.Gly1655Glu
|
|
ENST00000638510.1:n.3277G>A
|
|
|
ENST00000639431.1:c.265+135061G>A
|
ENSP00000491057.1:n.265+135061G>A
|
|
ENST00000640407.1:c.2420G>A
|
ENSP00000491425.1:p.Gly807Glu
|
|
XM_011543675.1:c.16007G>A
|
XP_011541977.1:p.Gly5336Glu
|
|
XM_011543676.1:c.15929G>A
|
XP_011541978.1:p.Gly5310Glu
|
|
XM_011543677.1:c.13313G>A
|
XP_011541979.1:p.Gly4438Glu
|
|
XM_017009963.2:c.16031G>A
|
XP_016865452.1:p.Gly5344Glu
|
|
XM_017009964.2:c.16028G>A
|
XP_016865453.1:p.Gly5343Glu
|
|
XM_017009965.1:c.16028G>A
|
XP_016865454.1:p.Gly5343Glu
|
|
XM_017009966.2:c.15950G>A
|
XP_016865455.1:p.Gly5317Glu
|
|
XM_017009967.1:c.15935G>A
|
XP_016865456.1:p.Gly5312Glu
|
|
XM_017009968.2:c.15851G>A
|
XP_016865457.1:p.Gly5284Glu
|
|
XM_017009969.2:c.16031G>A
|
XP_016865458.1:p.Gly5344Glu
|
|
XM_017009972.1:c.9149G>A
|
XP_016865461.1:p.Gly3050Glu
|
|
XM_017009973.1:c.9128G>A
|
XP_016865462.1:p.Gly3043Glu
|