ENST00000261647.10:c.153C>G
MANE Select
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ENSP00000261647.5:p.Gly51=
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ENST00000261647.9:c.153C>G
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ENSP00000261647.5:p.Gly51=
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ENST00000466729.5:c.218C>G
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ENST00000470399.1:c.168C>G
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ENSP00000465082.1:p.Gly56=
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ENST00000475723.5:c.200C>G
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ENST00000497842.6:n.178C>G
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ENST00000583704.1:n.178C>G
|
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NM_001271420.1:c.-306C>G
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NP_001258349.1:n.-306C>G
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NM_017775.3:c.153C>G
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NP_060245.3:p.Gly51=
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XM_011523950.1:c.153C>G
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XP_011522252.1:p.Gly51=
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XM_017024801.2:c.153C>G
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XP_016880290.2:p.Gly51=
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XM_017024802.2:c.153C>G
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XP_016880291.2:p.Gly51=
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XM_024450814.1:c.153C>G
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XP_024306582.1:p.Gly51=
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NM_017775.4:c.153C>G
MANE Select
|
NP_060245.3:p.Gly51=
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NM_001271420.2:c.-306C>G
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NP_001258349.1:n.-306C>G
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