|
NM_032119.4:c.8347G>T
MANE Select
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NP_115495.3:p.Glu2783Ter
|
|
ENST00000405460.9:c.8347G>T
MANE Select
|
ENSP00000384582.2:p.Glu2783Ter
|
|
NM_032119.3:c.8347G>T
|
NP_115495.3:p.Glu2783Ter
|
|
NR_003149.1:n.8360G>T
|
|
|
NR_003149.2:n.8363G>T
|
|
|
ENST00000405460.6:c.8347G>T
|
ENSP00000384582.2:p.Glu2783Ter
|
|
ENST00000509621.1:c.1044G>T
|
|
|
ENST00000639431.1:c.265+28240G>T
|
ENSP00000491057.1:n.265+28240G>T
|
|
ENST00000639473.1:n.3806G>T
|
|
|
ENST00000640012.1:c.2154G>T
|
|
|
ENST00000640374.1:n.1491G>T
|
|
|
ENST00000640403.1:c.5638G>T
|
ENSP00000492531.1:p.Glu1880Ter
|
|
ENST00000640779.1:c.3076G>T
|
|
|
XM_011543675.1:c.8344G>T
|
XP_011541977.1:p.Glu2782Ter
|
|
XM_011543676.1:c.8266G>T
|
XP_011541978.1:p.Glu2756Ter
|
|
XM_011543677.1:c.5650G>T
|
XP_011541979.1:p.Glu1884Ter
|
|
XM_011543678.1:c.8347G>T
|
XP_011541980.1:p.Glu2783Ter
|
|
XM_011543679.1:c.8347G>T
|
XP_011541981.1:p.Glu2783Ter
|
|
XM_017009963.2:c.8347G>T
|
XP_016865452.1:p.Glu2783Ter
|
|
XM_017009964.2:c.8344G>T
|
XP_016865453.1:p.Glu2782Ter
|
|
XM_017009965.1:c.8344G>T
|
XP_016865454.1:p.Glu2782Ter
|
|
XM_017009966.2:c.8266G>T
|
XP_016865455.1:p.Glu2756Ter
|
|
XM_017009967.1:c.8251G>T
|
XP_016865456.1:p.Glu2751Ter
|
|
XM_017009968.2:c.8347G>T
|
XP_016865457.1:p.Glu2783Ter
|
|
XM_017009969.2:c.8347G>T
|
XP_016865458.1:p.Glu2783Ter
|
|
XM_017009970.2:c.8347G>T
|
XP_016865459.1:p.Glu2783Ter
|
|
XM_017009971.2:c.8347G>T
|
XP_016865460.1:p.Glu2783Ter
|
|
XM_017009972.1:c.1465G>T
|
XP_016865461.1:p.Glu489Ter
|
|
XM_017009973.1:c.1465G>T
|
XP_016865462.1:p.Glu489Ter
|
|
XM_017009974.2:c.8347G>T
|
XP_016865463.1:p.Glu2783Ter
|