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NM_032119.4:c.13757A>G
MANE Select
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NP_115495.3:p.Glu4586Gly
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ENST00000405460.9:c.13757A>G
MANE Select
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ENSP00000384582.2:p.Glu4586Gly
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NM_032119.3:c.13757A>G
|
NP_115495.3:p.Glu4586Gly
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NR_003149.1:n.13770A>G
|
|
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NR_003149.2:n.13773A>G
|
|
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ENST00000405460.6:c.13757A>G
|
ENSP00000384582.2:p.Glu4586Gly
|
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ENST00000425867.2:c.740A>G
|
ENSP00000392618.2:p.Glu247Gly
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ENST00000425867.3:c.2711A>G
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ENSP00000392618.3:p.Glu904Gly
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ENST00000638510.1:n.1024A>G
|
|
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ENST00000638975.1:c.386A>G
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ENSP00000492630.1:p.Glu129Gly
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ENST00000639431.1:c.265+111965A>G
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ENSP00000491057.1:n.265+111965A>G
|
|
ENST00000640407.1:c.167A>G
|
ENSP00000491425.1:p.Glu56Gly
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XM_011543675.1:c.13754A>G
|
XP_011541977.1:p.Glu4585Gly
|
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XM_011543676.1:c.13676A>G
|
XP_011541978.1:p.Glu4559Gly
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XM_011543677.1:c.11060A>G
|
XP_011541979.1:p.Glu3687Gly
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XM_011543678.1:c.13757A>G
|
XP_011541980.1:p.Glu4586Gly
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XM_017009963.2:c.13778A>G
|
XP_016865452.1:p.Glu4593Gly
|
|
XM_017009964.2:c.13775A>G
|
XP_016865453.1:p.Glu4592Gly
|
|
XM_017009965.1:c.13775A>G
|
XP_016865454.1:p.Glu4592Gly
|
|
XM_017009966.2:c.13697A>G
|
XP_016865455.1:p.Glu4566Gly
|
|
XM_017009967.1:c.13682A>G
|
XP_016865456.1:p.Glu4561Gly
|
|
XM_017009968.2:c.13778A>G
|
XP_016865457.1:p.Glu4593Gly
|
|
XM_017009969.2:c.13778A>G
|
XP_016865458.1:p.Glu4593Gly
|
|
XM_017009970.2:c.13778A>G
|
XP_016865459.1:p.Glu4593Gly
|
|
XM_017009971.2:c.13778A>G
|
XP_016865460.1:p.Glu4593Gly
|
|
XM_017009972.1:c.6896A>G
|
XP_016865461.1:p.Glu2299Gly
|
|
XM_017009973.1:c.6875A>G
|
XP_016865462.1:p.Glu2292Gly
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