ENST00000280097.5:c.525A>G
MANE Select
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ENSP00000280097.3:p.Gly175=
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ENST00000280097.4:c.525A>G
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ENSP00000280097.3:p.Gly175=
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ENST00000410115.5:c.525A>G
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ENSP00000386940.1:p.Gly175=
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ENST00000485653.1:n.457A>G
|
|
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NM_006895.2:c.525A>G
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NP_008826.1:p.Gly175=
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XM_011511063.1:c.423A>G
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XP_011509365.1:p.Gly141=
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XM_011511064.1:c.147A>G
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XP_011509366.1:p.Gly49=
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XM_011511064.2:c.147A>G
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XP_011509366.1:p.Gly49=
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XM_017003948.1:c.423A>G
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XP_016859437.1:p.Gly141=
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XR_001739719.1:n.232-5980T>C
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|
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XR_002959286.1:n.912A>G
|
|
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NM_006895.3:c.525A>G
MANE Select
|
NP_008826.1:p.Gly175=
|
|