ENST00000220616.9:c.8077G>A
MANE Select
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ENSP00000220616.4:p.Gly2693Ser
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ENST00000220616.8:c.8077G>A
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ENSP00000220616.4:p.Gly2693Ser
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ENST00000519178.5:c.3443G>A
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ENST00000519543.5:c.2476G>A
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ENSP00000430430.1:p.Gly826Ser
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ENST00000521107.1:c.289G>A
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ENSP00000430161.1:p.Gly97Ser
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ENST00000522691.1:n.163G>A
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|
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ENST00000523756.5:c.4732G>A
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NM_003235.4:c.8077G>A
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NP_003226.4:p.Gly2693Ser
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XM_005251038.3:c.7885G>A
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XP_005251095.1:p.Gly2629Ser
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XM_006716622.2:c.8014G>A
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XP_006716685.1:p.Gly2672Ser
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XM_005251038.4:c.7885G>A
|
XP_005251095.1:p.Gly2629Ser
|
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XM_006716622.3:c.8014G>A
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XP_006716685.1:p.Gly2672Ser
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XM_017013793.1:c.8011G>A
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XP_016869282.1:p.Gly2671Ser
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XM_017013794.1:c.7942G>A
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XP_016869283.1:p.Gly2648Ser
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XM_017013795.1:c.7906G>A
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XP_016869284.1:p.Gly2636Ser
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XM_017013796.1:c.7858G>A
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XP_016869285.1:p.Gly2620Ser
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XM_017013797.1:c.7816G>A
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XP_016869286.1:p.Gly2606Ser
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NM_003235.5:c.8077G>A
MANE Select
|
NP_003226.4:p.Gly2693Ser
|
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