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NM_032119.4:c.10997A>G
MANE Select
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NP_115495.3:p.Glu3666Gly
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ENST00000405460.9:c.10997A>G
MANE Select
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ENSP00000384582.2:p.Glu3666Gly
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NM_032119.3:c.10997A>G
|
NP_115495.3:p.Glu3666Gly
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NR_003149.1:n.11010A>G
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NR_003149.2:n.11013A>G
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ENST00000405460.6:c.10997A>G
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ENSP00000384582.2:p.Glu3666Gly
|
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ENST00000425867.3:c.128A>G
|
ENSP00000392618.3:p.Glu43Gly
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ENST00000509621.1:c.3694A>G
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ENST00000639431.1:c.265+74364A>G
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ENSP00000491057.1:n.265+74364A>G
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ENST00000640374.1:n.4141A>G
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ENST00000640464.1:n.1416A>G
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XM_011543675.1:c.10994A>G
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XP_011541977.1:p.Glu3665Gly
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XM_011543676.1:c.10916A>G
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XP_011541978.1:p.Glu3639Gly
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XM_011543677.1:c.8300A>G
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XP_011541979.1:p.Glu2767Gly
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XM_011543678.1:c.10997A>G
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XP_011541980.1:p.Glu3666Gly
|
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XM_017009963.2:c.11018A>G
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XP_016865452.1:p.Glu3673Gly
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XM_017009964.2:c.11015A>G
|
XP_016865453.1:p.Glu3672Gly
|
|
XM_017009965.1:c.11015A>G
|
XP_016865454.1:p.Glu3672Gly
|
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XM_017009966.2:c.10937A>G
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XP_016865455.1:p.Glu3646Gly
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XM_017009967.1:c.10922A>G
|
XP_016865456.1:p.Glu3641Gly
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XM_017009968.2:c.11018A>G
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XP_016865457.1:p.Glu3673Gly
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|
XM_017009969.2:c.11018A>G
|
XP_016865458.1:p.Glu3673Gly
|
|
XM_017009970.2:c.11018A>G
|
XP_016865459.1:p.Glu3673Gly
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XM_017009971.2:c.11018A>G
|
XP_016865460.1:p.Glu3673Gly
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XM_017009972.1:c.4136A>G
|
XP_016865461.1:p.Glu1379Gly
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XM_017009973.1:c.4115A>G
|
XP_016865462.1:p.Glu1372Gly
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