ENST00000405460.9:c.8655T>A
MANE Select
|
ENSP00000384582.2:p.Asp2885Glu
|
|
ENST00000639431.1:c.265+30110T>A
|
ENSP00000491057.1:n.265+30110T>A
|
|
ENST00000639473.1:n.4114T>A
|
|
|
ENST00000640012.1:c.2462T>A
|
|
|
ENST00000640374.1:n.1799T>A
|
|
|
ENST00000640403.1:c.5946T>A
|
ENSP00000492531.1:p.Asp1982Glu
|
|
ENST00000640779.1:c.3384T>A
|
|
|
ENST00000405460.6:c.8655T>A
|
ENSP00000384582.2:p.Asp2885Glu
|
|
ENST00000509621.1:c.1352T>A
|
|
|
NM_032119.3:c.8655T>A
|
NP_115495.3:p.Asp2885Glu
|
|
NR_003149.1:n.8668T>A
|
|
|
XM_011543675.1:c.8652T>A
|
XP_011541977.1:p.Asp2884Glu
|
|
XM_011543676.1:c.8574T>A
|
XP_011541978.1:p.Asp2858Glu
|
|
XM_011543677.1:c.5958T>A
|
XP_011541979.1:p.Asp1986Glu
|
|
XM_011543678.1:c.8655T>A
|
XP_011541980.1:p.Asp2885Glu
|
|
XM_011543679.1:c.8655T>A
|
XP_011541981.1:p.Asp2885Glu
|
|
NM_032119.4:c.8655T>A
MANE Select
|
NP_115495.3:p.Asp2885Glu
|
|
XM_017009963.2:c.8676T>A
|
XP_016865452.1:p.Asp2892Glu
|
|
XM_017009964.2:c.8673T>A
|
XP_016865453.1:p.Asp2891Glu
|
|
XM_017009965.1:c.8673T>A
|
XP_016865454.1:p.Asp2891Glu
|
|
XM_017009966.2:c.8595T>A
|
XP_016865455.1:p.Asp2865Glu
|
|
XM_017009967.1:c.8580T>A
|
XP_016865456.1:p.Asp2860Glu
|
|
XM_017009968.2:c.8676T>A
|
XP_016865457.1:p.Asp2892Glu
|
|
XM_017009969.2:c.8676T>A
|
XP_016865458.1:p.Asp2892Glu
|
|
XM_017009970.2:c.8676T>A
|
XP_016865459.1:p.Asp2892Glu
|
|
XM_017009971.2:c.8676T>A
|
XP_016865460.1:p.Asp2892Glu
|
|
XM_017009972.1:c.1794T>A
|
XP_016865461.1:p.Asp598Glu
|
|
XM_017009973.1:c.1773T>A
|
XP_016865462.1:p.Asp591Glu
|
|
XM_017009974.2:c.8676T>A
|
XP_016865463.1:p.Asp2892Glu
|
|
NR_003149.2:n.8671T>A
|
|
|