ENST00000405460.9:c.10798G=
MANE Select
|
ENSP00000384582.2:p.Glu3600=
|
|
ENST00000639431.1:c.265+69410G=
|
ENSP00000491057.1:n.265+69410G=
|
|
ENST00000640374.1:n.3942G=
|
|
|
ENST00000640464.1:n.1217G=
|
|
|
ENST00000405460.6:c.10798G=
|
ENSP00000384582.2:p.Glu3600=
|
|
ENST00000509621.1:c.3495G=
|
|
|
NM_032119.3:c.10798G=
|
NP_115495.3:p.Glu3600=
|
|
NR_003149.1:n.10811G=
|
|
|
XM_011543675.1:c.10795G=
|
XP_011541977.1:p.Glu3599=
|
|
XM_011543676.1:c.10717G=
|
XP_011541978.1:p.Glu3573=
|
|
XM_011543677.1:c.8101G=
|
XP_011541979.1:p.Glu2701=
|
|
XM_011543678.1:c.10798G=
|
XP_011541980.1:p.Glu3600=
|
|
XM_011543679.1:c.*20G=
|
XP_011541981.1:n.*20G=
|
|
NM_032119.4:c.10798G=
MANE Select
|
NP_115495.3:p.Glu3600=
|
|
XM_017009963.2:c.10819G=
|
XP_016865452.1:p.Glu3607=
|
|
XM_017009964.2:c.10816G=
|
XP_016865453.1:p.Glu3606=
|
|
XM_017009965.1:c.10816G=
|
XP_016865454.1:p.Glu3606=
|
|
XM_017009966.2:c.10738G=
|
XP_016865455.1:p.Glu3580=
|
|
XM_017009967.1:c.10723G=
|
XP_016865456.1:p.Glu3575=
|
|
XM_017009968.2:c.10819G=
|
XP_016865457.1:p.Glu3607=
|
|
XM_017009969.2:c.10819G=
|
XP_016865458.1:p.Glu3607=
|
|
XM_017009970.2:c.10819G=
|
XP_016865459.1:p.Glu3607=
|
|
XM_017009971.2:c.10819G=
|
XP_016865460.1:p.Glu3607=
|
|
XM_017009972.1:c.3937G=
|
XP_016865461.1:p.Glu1313=
|
|
XM_017009973.1:c.3916G=
|
XP_016865462.1:p.Glu1306=
|
|
XM_017009974.2:c.*20G=
|
XP_016865463.1:n.*20G=
|
|
NR_003149.2:n.10814G=
|
|
|