ENST00000456935.7:c.1780C>A
MANE Select
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ENSP00000395473.2:p.Gln594Lys
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|
ENST00000221363.8:c.1777C>A
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ENSP00000221363.4:p.Gln593Lys
|
|
ENST00000433513.5:n.386C>A
|
|
|
ENST00000456935.6:c.1780C>A
|
ENSP00000395473.2:p.Gln594Lys
|
|
ENST00000466794.5:n.2370C>A
|
|
|
ENST00000593686.1:c.373C>A
|
|
|
ENST00000595880.5:n.377C>A
|
|
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ENST00000596591.1:c.144C>A
|
|
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NM_000528.3:c.1780C>A
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NP_000519.2:p.Gln594Lys
|
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NM_001173498.1:c.1777C>A
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NP_001166969.1:p.Gln593Lys
|
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XM_005259913.1:c.1783C>A
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XP_005259970.1:p.Gln595Lys
|
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XM_011528017.1:c.679C>A
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XP_011526319.1:p.Gln227Lys
|
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XM_005259913.2:c.1783C>A
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XP_005259970.1:p.Gln595Lys
|
|
XM_024451518.1:c.679C>A
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XP_024307286.1:p.Gln227Lys
|
|
NM_000528.4:c.1780C>A
MANE Select
|
NP_000519.2:p.Gln594Lys
|
|
NM_001173498.2:c.1777C>A
|
NP_001166969.1:p.Gln593Lys
|
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