ENST00000220616.9:c.8066T>G
MANE Select
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ENSP00000220616.4:p.Val2689Gly
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ENST00000220616.8:c.8066T>G
|
ENSP00000220616.4:p.Val2689Gly
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|
ENST00000519178.5:c.3432T>G
|
|
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ENST00000519543.5:c.2465T>G
|
ENSP00000430430.1:p.Val822Gly
|
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ENST00000521107.1:c.278T>G
|
ENSP00000430161.1:p.Val93Gly
|
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ENST00000522691.1:n.152T>G
|
|
|
ENST00000523756.5:c.4721T>G
|
|
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NM_003235.4:c.8066T>G
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NP_003226.4:p.Val2689Gly
|
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XM_005251038.3:c.7874T>G
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XP_005251095.1:p.Val2625Gly
|
|
XM_006716622.2:c.8003T>G
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XP_006716685.1:p.Val2668Gly
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XM_005251038.4:c.7874T>G
|
XP_005251095.1:p.Val2625Gly
|
|
XM_006716622.3:c.8003T>G
|
XP_006716685.1:p.Val2668Gly
|
|
XM_017013793.1:c.8000T>G
|
XP_016869282.1:p.Val2667Gly
|
|
XM_017013794.1:c.7931T>G
|
XP_016869283.1:p.Val2644Gly
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|
XM_017013795.1:c.7895T>G
|
XP_016869284.1:p.Val2632Gly
|
|
XM_017013796.1:c.7847T>G
|
XP_016869285.1:p.Val2616Gly
|
|
XM_017013797.1:c.7805T>G
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XP_016869286.1:p.Val2602Gly
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NM_003235.5:c.8066T>G
MANE Select
|
NP_003226.4:p.Val2689Gly
|
|