ENST00000405460.9:c.11518G>C
MANE Select
|
ENSP00000384582.2:p.Glu3840Gln
|
|
ENST00000425867.3:c.649G>C
|
ENSP00000392618.3:p.Glu217Gln
|
|
ENST00000639431.1:c.265+78914G>C
|
ENSP00000491057.1:n.265+78914G>C
|
|
ENST00000640374.1:n.4662G>C
|
|
|
ENST00000640464.1:n.1937G>C
|
|
|
ENST00000405460.6:c.11518G>C
|
ENSP00000384582.2:p.Glu3840Gln
|
|
ENST00000509621.1:c.4215G>C
|
|
|
NM_032119.3:c.11518G>C
|
NP_115495.3:p.Glu3840Gln
|
|
NR_003149.1:n.11531G>C
|
|
|
XM_011543675.1:c.11515G>C
|
XP_011541977.1:p.Glu3839Gln
|
|
XM_011543676.1:c.11437G>C
|
XP_011541978.1:p.Glu3813Gln
|
|
XM_011543677.1:c.8821G>C
|
XP_011541979.1:p.Glu2941Gln
|
|
XM_011543678.1:c.11518G>C
|
XP_011541980.1:p.Glu3840Gln
|
|
NM_032119.4:c.11518G>C
MANE Select
|
NP_115495.3:p.Glu3840Gln
|
|
XM_017009963.2:c.11539G>C
|
XP_016865452.1:p.Glu3847Gln
|
|
XM_017009964.2:c.11536G>C
|
XP_016865453.1:p.Glu3846Gln
|
|
XM_017009965.1:c.11536G>C
|
XP_016865454.1:p.Glu3846Gln
|
|
XM_017009966.2:c.11458G>C
|
XP_016865455.1:p.Glu3820Gln
|
|
XM_017009967.1:c.11443G>C
|
XP_016865456.1:p.Glu3815Gln
|
|
XM_017009968.2:c.11539G>C
|
XP_016865457.1:p.Glu3847Gln
|
|
XM_017009969.2:c.11539G>C
|
XP_016865458.1:p.Glu3847Gln
|
|
XM_017009970.2:c.11539G>C
|
XP_016865459.1:p.Glu3847Gln
|
|
XM_017009971.2:c.11539G>C
|
XP_016865460.1:p.Glu3847Gln
|
|
XM_017009972.1:c.4657G>C
|
XP_016865461.1:p.Glu1553Gln
|
|
XM_017009973.1:c.4636G>C
|
XP_016865462.1:p.Glu1546Gln
|
|
NR_003149.2:n.11534G>C
|
|
|