ENST00000405460.9:c.11539G>T
MANE Select
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ENSP00000384582.2:p.Glu3847Ter
|
|
ENST00000425867.3:c.670G>T
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ENSP00000392618.3:p.Glu224Ter
|
|
ENST00000639431.1:c.265+78935G>T
|
ENSP00000491057.1:n.265+78935G>T
|
|
ENST00000640374.1:n.4683G>T
|
|
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ENST00000640464.1:n.1958G>T
|
|
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ENST00000405460.6:c.11539G>T
|
ENSP00000384582.2:p.Glu3847Ter
|
|
ENST00000509621.1:c.4236G>T
|
|
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NM_032119.3:c.11539G>T
|
NP_115495.3:p.Glu3847Ter
|
|
NR_003149.1:n.11552G>T
|
|
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XM_011543675.1:c.11536G>T
|
XP_011541977.1:p.Glu3846Ter
|
|
XM_011543676.1:c.11458G>T
|
XP_011541978.1:p.Glu3820Ter
|
|
XM_011543677.1:c.8842G>T
|
XP_011541979.1:p.Glu2948Ter
|
|
XM_011543678.1:c.11539G>T
|
XP_011541980.1:p.Glu3847Ter
|
|
NM_032119.4:c.11539G>T
MANE Select
|
NP_115495.3:p.Glu3847Ter
|
|
XM_017009963.2:c.11560G>T
|
XP_016865452.1:p.Glu3854Ter
|
|
XM_017009964.2:c.11557G>T
|
XP_016865453.1:p.Glu3853Ter
|
|
XM_017009965.1:c.11557G>T
|
XP_016865454.1:p.Glu3853Ter
|
|
XM_017009966.2:c.11479G>T
|
XP_016865455.1:p.Glu3827Ter
|
|
XM_017009967.1:c.11464G>T
|
XP_016865456.1:p.Glu3822Ter
|
|
XM_017009968.2:c.11560G>T
|
XP_016865457.1:p.Glu3854Ter
|
|
XM_017009969.2:c.11560G>T
|
XP_016865458.1:p.Glu3854Ter
|
|
XM_017009970.2:c.11560G>T
|
XP_016865459.1:p.Glu3854Ter
|
|
XM_017009971.2:c.11560G>T
|
XP_016865460.1:p.Glu3854Ter
|
|
XM_017009972.1:c.4678G>T
|
XP_016865461.1:p.Glu1560Ter
|
|
XM_017009973.1:c.4657G>T
|
XP_016865462.1:p.Glu1553Ter
|
|
NR_003149.2:n.11555G>T
|
|
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