ENST00000405460.9:c.11539G>A
MANE Select
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ENSP00000384582.2:p.Glu3847Lys
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ENST00000425867.3:c.670G>A
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ENSP00000392618.3:p.Glu224Lys
|
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ENST00000639431.1:c.265+78935G>A
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ENSP00000491057.1:n.265+78935G>A
|
|
ENST00000640374.1:n.4683G>A
|
|
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ENST00000640464.1:n.1958G>A
|
|
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ENST00000405460.6:c.11539G>A
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ENSP00000384582.2:p.Glu3847Lys
|
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ENST00000509621.1:c.4236G>A
|
|
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NM_032119.3:c.11539G>A
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NP_115495.3:p.Glu3847Lys
|
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NR_003149.1:n.11552G>A
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|
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XM_011543675.1:c.11536G>A
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XP_011541977.1:p.Glu3846Lys
|
|
XM_011543676.1:c.11458G>A
|
XP_011541978.1:p.Glu3820Lys
|
|
XM_011543677.1:c.8842G>A
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XP_011541979.1:p.Glu2948Lys
|
|
XM_011543678.1:c.11539G>A
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XP_011541980.1:p.Glu3847Lys
|
|
NM_032119.4:c.11539G>A
MANE Select
|
NP_115495.3:p.Glu3847Lys
|
|
XM_017009963.2:c.11560G>A
|
XP_016865452.1:p.Glu3854Lys
|
|
XM_017009964.2:c.11557G>A
|
XP_016865453.1:p.Glu3853Lys
|
|
XM_017009965.1:c.11557G>A
|
XP_016865454.1:p.Glu3853Lys
|
|
XM_017009966.2:c.11479G>A
|
XP_016865455.1:p.Glu3827Lys
|
|
XM_017009967.1:c.11464G>A
|
XP_016865456.1:p.Glu3822Lys
|
|
XM_017009968.2:c.11560G>A
|
XP_016865457.1:p.Glu3854Lys
|
|
XM_017009969.2:c.11560G>A
|
XP_016865458.1:p.Glu3854Lys
|
|
XM_017009970.2:c.11560G>A
|
XP_016865459.1:p.Glu3854Lys
|
|
XM_017009971.2:c.11560G>A
|
XP_016865460.1:p.Glu3854Lys
|
|
XM_017009972.1:c.4678G>A
|
XP_016865461.1:p.Glu1560Lys
|
|
XM_017009973.1:c.4657G>A
|
XP_016865462.1:p.Glu1553Lys
|
|
NR_003149.2:n.11555G>A
|
|
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