ENST00000456935.7:c.2727C>G
MANE Select
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ENSP00000395473.2:p.Gly909=
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ENST00000221363.8:c.2724C>G
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ENSP00000221363.4:p.Gly908=
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ENST00000456935.6:c.2727C>G
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ENSP00000395473.2:p.Gly909=
|
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ENST00000466794.5:n.3317C>G
|
|
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ENST00000469423.1:n.49C>G
|
|
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ENST00000493218.5:n.138C>G
|
|
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ENST00000597692.1:c.286C>G
|
|
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NM_000528.3:c.2727C>G
|
NP_000519.2:p.Gly909=
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NM_001173498.1:c.2724C>G
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NP_001166969.1:p.Gly908=
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XM_005259913.1:c.2730C>G
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XP_005259970.1:p.Gly910=
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XM_011528017.1:c.1626C>G
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XP_011526319.1:p.Gly542=
|
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XM_005259913.2:c.2730C>G
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XP_005259970.1:p.Gly910=
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XM_024451518.1:c.1626C>G
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XP_024307286.1:p.Gly542=
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|
NM_000528.4:c.2727C>G
MANE Select
|
NP_000519.2:p.Gly909=
|
|
NM_001173498.2:c.2724C>G
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NP_001166969.1:p.Gly908=
|
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