ENST00000553106.6:c.36C>G
MANE Select
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ENSP00000448059.1:p.Gly12=
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ENST00000307000.7:c.-112C>G
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ENSP00000303500.2:n.-112C>G
|
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ENST00000546844.1:c.36C>G
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ENSP00000446658.1:p.Gly12=
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ENST00000547319.1:n.347C>G
|
|
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ENST00000549111.5:n.132C>G
|
|
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ENST00000550978.6:c.20C>G
|
|
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ENST00000551337.5:c.36C>G
|
ENSP00000447620.1:p.Gly12=
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ENST00000551988.5:n.125C>G
|
|
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ENST00000553106.5:c.36C>G
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ENSP00000448059.1:p.Gly12=
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ENST00000635500.1:n.29-4197C>G
|
|
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NM_000277.1:c.36C>G
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NP_000268.1:p.Gly12=
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XM_011538422.1:c.36C>G
|
XP_011536724.1:p.Gly12=
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NM_000277.2:c.36C>G
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NP_000268.1:p.Gly12=
|
|
NM_001354304.1:c.36C>G
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NP_001341233.1:p.Gly12=
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XM_017019370.2:c.36C>G
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XP_016874859.1:p.Gly12=
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NM_000277.3:c.36C>G
MANE Select
|
NP_000268.1:p.Gly12=
|
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NM_001354304.2:c.36C>G
|
NP_001341233.1:p.Gly12=
|
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