ENST00000456935.7:c.1455C>G
MANE Select
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ENSP00000395473.2:p.Gly485=
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ENST00000221363.8:c.1452C>G
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ENSP00000221363.4:p.Gly484=
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ENST00000433513.5:n.61C>G
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|
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ENST00000456935.6:c.1455C>G
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ENSP00000395473.2:p.Gly485=
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ENST00000466794.5:n.1354C>G
|
|
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ENST00000495617.1:n.631C>G
|
|
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ENST00000593686.1:c.65C>G
|
|
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ENST00000595880.5:n.52C>G
|
|
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NM_000528.3:c.1455C>G
|
NP_000519.2:p.Gly485=
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NM_001173498.1:c.1452C>G
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NP_001166969.1:p.Gly484=
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XM_005259913.1:c.1458C>G
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XP_005259970.1:p.Gly486=
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XM_011528017.1:c.354C>G
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XP_011526319.1:p.Gly118=
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XM_005259913.2:c.1458C>G
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XP_005259970.1:p.Gly486=
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XM_024451518.1:c.354C>G
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XP_024307286.1:p.Gly118=
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|
NM_000528.4:c.1455C>G
MANE Select
|
NP_000519.2:p.Gly485=
|
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NM_001173498.2:c.1452C>G
|
NP_001166969.1:p.Gly484=
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