ENST00000405460.9:c.11520A>C
MANE Select
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ENSP00000384582.2:p.Glu3840Asp
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ENST00000425867.3:c.651A>C
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ENSP00000392618.3:p.Glu217Asp
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ENST00000639431.1:c.265+78916A>C
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ENSP00000491057.1:n.265+78916A>C
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ENST00000640374.1:n.4664A>C
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|
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ENST00000640464.1:n.1939A>C
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ENST00000405460.6:c.11520A>C
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ENSP00000384582.2:p.Glu3840Asp
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ENST00000509621.1:c.4217A>C
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|
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NM_032119.3:c.11520A>C
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NP_115495.3:p.Glu3840Asp
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NR_003149.1:n.11533A>C
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XM_011543675.1:c.11517A>C
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XP_011541977.1:p.Glu3839Asp
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XM_011543676.1:c.11439A>C
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XP_011541978.1:p.Glu3813Asp
|
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XM_011543677.1:c.8823A>C
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XP_011541979.1:p.Glu2941Asp
|
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XM_011543678.1:c.11520A>C
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XP_011541980.1:p.Glu3840Asp
|
|
NM_032119.4:c.11520A>C
MANE Select
|
NP_115495.3:p.Glu3840Asp
|
|
XM_017009963.2:c.11541A>C
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XP_016865452.1:p.Glu3847Asp
|
|
XM_017009964.2:c.11538A>C
|
XP_016865453.1:p.Glu3846Asp
|
|
XM_017009965.1:c.11538A>C
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XP_016865454.1:p.Glu3846Asp
|
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XM_017009966.2:c.11460A>C
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XP_016865455.1:p.Glu3820Asp
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XM_017009967.1:c.11445A>C
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XP_016865456.1:p.Glu3815Asp
|
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XM_017009968.2:c.11541A>C
|
XP_016865457.1:p.Glu3847Asp
|
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XM_017009969.2:c.11541A>C
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XP_016865458.1:p.Glu3847Asp
|
|
XM_017009970.2:c.11541A>C
|
XP_016865459.1:p.Glu3847Asp
|
|
XM_017009971.2:c.11541A>C
|
XP_016865460.1:p.Glu3847Asp
|
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XM_017009972.1:c.4659A>C
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XP_016865461.1:p.Glu1553Asp
|
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XM_017009973.1:c.4638A>C
|
XP_016865462.1:p.Glu1546Asp
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NR_003149.2:n.11536A>C
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