ENST00000220616.9:c.8113C>G
MANE Select
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ENSP00000220616.4:p.Pro2705Ala
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ENST00000220616.8:c.8113C>G
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ENSP00000220616.4:p.Pro2705Ala
|
|
ENST00000519178.5:c.3479C>G
|
|
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ENST00000519543.5:c.2512C>G
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ENSP00000430430.1:p.Pro838Ala
|
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ENST00000521107.1:c.325C>G
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ENSP00000430161.1:p.Pro109Ala
|
|
ENST00000522691.1:n.199C>G
|
|
|
ENST00000523756.5:c.4768C>G
|
|
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NM_003235.4:c.8113C>G
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NP_003226.4:p.Pro2705Ala
|
|
XM_005251038.3:c.7921C>G
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XP_005251095.1:p.Pro2641Ala
|
|
XM_006716622.2:c.8050C>G
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XP_006716685.1:p.Pro2684Ala
|
|
XM_005251038.4:c.7921C>G
|
XP_005251095.1:p.Pro2641Ala
|
|
XM_006716622.3:c.8050C>G
|
XP_006716685.1:p.Pro2684Ala
|
|
XM_017013793.1:c.8047C>G
|
XP_016869282.1:p.Pro2683Ala
|
|
XM_017013794.1:c.7978C>G
|
XP_016869283.1:p.Pro2660Ala
|
|
XM_017013795.1:c.7942C>G
|
XP_016869284.1:p.Pro2648Ala
|
|
XM_017013796.1:c.7894C>G
|
XP_016869285.1:p.Pro2632Ala
|
|
XM_017013797.1:c.7852C>G
|
XP_016869286.1:p.Pro2618Ala
|
|
NM_003235.5:c.8113C>G
MANE Select
|
NP_003226.4:p.Pro2705Ala
|
|