ENST00000405460.9:c.10854A>C
MANE Select
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ENSP00000384582.2:p.Glu3618Asp
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ENST00000639431.1:c.265+69466A>C
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ENSP00000491057.1:n.265+69466A>C
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ENST00000640374.1:n.3998A>C
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|
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ENST00000640464.1:n.1273A>C
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|
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ENST00000405460.6:c.10854A>C
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ENSP00000384582.2:p.Glu3618Asp
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ENST00000509621.1:c.3551A>C
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|
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NM_032119.3:c.10854A>C
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NP_115495.3:p.Glu3618Asp
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NR_003149.1:n.10867A>C
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XM_011543675.1:c.10851A>C
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XP_011541977.1:p.Glu3617Asp
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XM_011543676.1:c.10773A>C
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XP_011541978.1:p.Glu3591Asp
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XM_011543677.1:c.8157A>C
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XP_011541979.1:p.Glu2719Asp
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XM_011543678.1:c.10854A>C
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XP_011541980.1:p.Glu3618Asp
|
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XM_011543679.1:c.*76A>C
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XP_011541981.1:n.*76A>C
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|
NM_032119.4:c.10854A>C
MANE Select
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NP_115495.3:p.Glu3618Asp
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|
XM_017009963.2:c.10875A>C
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XP_016865452.1:p.Glu3625Asp
|
|
XM_017009964.2:c.10872A>C
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XP_016865453.1:p.Glu3624Asp
|
|
XM_017009965.1:c.10872A>C
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XP_016865454.1:p.Glu3624Asp
|
|
XM_017009966.2:c.10794A>C
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XP_016865455.1:p.Glu3598Asp
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XM_017009967.1:c.10779A>C
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XP_016865456.1:p.Glu3593Asp
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XM_017009968.2:c.10875A>C
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XP_016865457.1:p.Glu3625Asp
|
|
XM_017009969.2:c.10875A>C
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XP_016865458.1:p.Glu3625Asp
|
|
XM_017009970.2:c.10875A>C
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XP_016865459.1:p.Glu3625Asp
|
|
XM_017009971.2:c.10875A>C
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XP_016865460.1:p.Glu3625Asp
|
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XM_017009972.1:c.3993A>C
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XP_016865461.1:p.Glu1331Asp
|
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XM_017009973.1:c.3972A>C
|
XP_016865462.1:p.Glu1324Asp
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XM_017009974.2:c.*76A>C
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XP_016865463.1:n.*76A>C
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NR_003149.2:n.10870A>C
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