|
NM_032119.4:c.18757G>T
MANE Select
|
NP_115495.3:p.Glu6253Ter
|
|
ENST00000405460.9:c.18757G>T
MANE Select
|
ENSP00000384582.2:p.Glu6253Ter
|
|
NM_032119.3:c.18757G>T
|
NP_115495.3:p.Glu6253Ter
|
|
NR_003149.1:n.18770G>T
|
|
|
NR_003149.2:n.18773G>T
|
|
|
ENST00000405460.6:c.18757G>T
|
ENSP00000384582.2:p.Glu6253Ter
|
|
ENST00000425867.2:c.5740G>T
|
ENSP00000392618.2:p.Glu1914Ter
|
|
ENST00000425867.3:c.7711G>T
|
ENSP00000392618.3:p.Glu2571Ter
|
|
ENST00000638510.1:n.6024G>T
|
|
|
ENST00000638990.1:c.1969G>T
|
|
|
ENST00000639212.1:n.677G>T
|
|
|
ENST00000639530.1:n.625G>T
|
|
|
ENST00000639821.1:c.517-10429G>T
|
ENSP00000492216.1:n.517-10429G>T
|
|
ENST00000640256.1:n.433G>T
|
|
|
ENST00000640407.1:c.5206G>T
|
ENSP00000491425.1:n.5206G>T
|
|
ENST00000640815.1:c.841G>T
|
ENSP00000491767.1:p.Glu281Ter
|
|
XM_011543675.1:c.18754G>T
|
XP_011541977.1:p.Glu6252Ter
|
|
XM_011543676.1:c.18676G>T
|
XP_011541978.1:p.Glu6226Ter
|
|
XM_011543677.1:c.16060G>T
|
XP_011541979.1:p.Glu5354Ter
|
|
XM_017009963.2:c.18778G>T
|
XP_016865452.1:p.Glu6260Ter
|
|
XM_017009964.2:c.18775G>T
|
XP_016865453.1:p.Glu6259Ter
|
|
XM_017009965.1:c.18775G>T
|
XP_016865454.1:p.Glu6259Ter
|
|
XM_017009966.2:c.18697G>T
|
XP_016865455.1:p.Glu6233Ter
|
|
XM_017009967.1:c.18682G>T
|
XP_016865456.1:p.Glu6228Ter
|
|
XM_017009968.2:c.18598G>T
|
XP_016865457.1:p.Glu6200Ter
|
|
XM_017009969.2:c.18454-10429G>T
|
XP_016865458.1:n.18454-10429G>T
|
|
XM_017009972.1:c.11896G>T
|
XP_016865461.1:p.Glu3966Ter
|
|
XM_017009973.1:c.11875G>T
|
XP_016865462.1:p.Glu3959Ter
|
|
XR_001742795.1:n.225-1165C>A
|
|
|
XR_001742796.1:n.225-17359C>A
|
|