ENST00000405460.9:c.10852G>T
MANE Select
|
ENSP00000384582.2:p.Glu3618Ter
|
|
ENST00000639431.1:c.265+69464G>T
|
ENSP00000491057.1:n.265+69464G>T
|
|
ENST00000640374.1:n.3996G>T
|
|
|
ENST00000640464.1:n.1271G>T
|
|
|
ENST00000405460.6:c.10852G>T
|
ENSP00000384582.2:p.Glu3618Ter
|
|
ENST00000509621.1:c.3549G>T
|
|
|
NM_032119.3:c.10852G>T
|
NP_115495.3:p.Glu3618Ter
|
|
NR_003149.1:n.10865G>T
|
|
|
XM_011543675.1:c.10849G>T
|
XP_011541977.1:p.Glu3617Ter
|
|
XM_011543676.1:c.10771G>T
|
XP_011541978.1:p.Glu3591Ter
|
|
XM_011543677.1:c.8155G>T
|
XP_011541979.1:p.Glu2719Ter
|
|
XM_011543678.1:c.10852G>T
|
XP_011541980.1:p.Glu3618Ter
|
|
XM_011543679.1:c.*74G>T
|
XP_011541981.1:n.*74G>T
|
|
NM_032119.4:c.10852G>T
MANE Select
|
NP_115495.3:p.Glu3618Ter
|
|
XM_017009963.2:c.10873G>T
|
XP_016865452.1:p.Glu3625Ter
|
|
XM_017009964.2:c.10870G>T
|
XP_016865453.1:p.Glu3624Ter
|
|
XM_017009965.1:c.10870G>T
|
XP_016865454.1:p.Glu3624Ter
|
|
XM_017009966.2:c.10792G>T
|
XP_016865455.1:p.Glu3598Ter
|
|
XM_017009967.1:c.10777G>T
|
XP_016865456.1:p.Glu3593Ter
|
|
XM_017009968.2:c.10873G>T
|
XP_016865457.1:p.Glu3625Ter
|
|
XM_017009969.2:c.10873G>T
|
XP_016865458.1:p.Glu3625Ter
|
|
XM_017009970.2:c.10873G>T
|
XP_016865459.1:p.Glu3625Ter
|
|
XM_017009971.2:c.10873G>T
|
XP_016865460.1:p.Glu3625Ter
|
|
XM_017009972.1:c.3991G>T
|
XP_016865461.1:p.Glu1331Ter
|
|
XM_017009973.1:c.3970G>T
|
XP_016865462.1:p.Glu1324Ter
|
|
XM_017009974.2:c.*74G>T
|
XP_016865463.1:n.*74G>T
|
|
NR_003149.2:n.10868G>T
|
|
|