ENST00000405460.9:c.10853A>G
MANE Select
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ENSP00000384582.2:p.Glu3618Gly
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ENST00000639431.1:c.265+69465A>G
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ENSP00000491057.1:n.265+69465A>G
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ENST00000640374.1:n.3997A>G
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ENST00000640464.1:n.1272A>G
|
|
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ENST00000405460.6:c.10853A>G
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ENSP00000384582.2:p.Glu3618Gly
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ENST00000509621.1:c.3550A>G
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NM_032119.3:c.10853A>G
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NP_115495.3:p.Glu3618Gly
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NR_003149.1:n.10866A>G
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XM_011543675.1:c.10850A>G
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XP_011541977.1:p.Glu3617Gly
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XM_011543676.1:c.10772A>G
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XP_011541978.1:p.Glu3591Gly
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XM_011543677.1:c.8156A>G
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XP_011541979.1:p.Glu2719Gly
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XM_011543678.1:c.10853A>G
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XP_011541980.1:p.Glu3618Gly
|
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XM_011543679.1:c.*75A>G
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XP_011541981.1:n.*75A>G
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NM_032119.4:c.10853A>G
MANE Select
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NP_115495.3:p.Glu3618Gly
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XM_017009963.2:c.10874A>G
|
XP_016865452.1:p.Glu3625Gly
|
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XM_017009964.2:c.10871A>G
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XP_016865453.1:p.Glu3624Gly
|
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XM_017009965.1:c.10871A>G
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XP_016865454.1:p.Glu3624Gly
|
|
XM_017009966.2:c.10793A>G
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XP_016865455.1:p.Glu3598Gly
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XM_017009967.1:c.10778A>G
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XP_016865456.1:p.Glu3593Gly
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XM_017009968.2:c.10874A>G
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XP_016865457.1:p.Glu3625Gly
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XM_017009969.2:c.10874A>G
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XP_016865458.1:p.Glu3625Gly
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XM_017009970.2:c.10874A>G
|
XP_016865459.1:p.Glu3625Gly
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XM_017009971.2:c.10874A>G
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XP_016865460.1:p.Glu3625Gly
|
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XM_017009972.1:c.3992A>G
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XP_016865461.1:p.Glu1331Gly
|
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XM_017009973.1:c.3971A>G
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XP_016865462.1:p.Glu1324Gly
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XM_017009974.2:c.*75A>G
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XP_016865463.1:n.*75A>G
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NR_003149.2:n.10869A>G
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