ENST00000220616.9:c.8109G=
MANE Select
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ENSP00000220616.4:p.Leu2703=
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ENST00000220616.8:c.8109G=
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ENSP00000220616.4:p.Leu2703=
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ENST00000519178.5:c.3475G=
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|
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ENST00000519543.5:c.2508G=
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ENSP00000430430.1:p.Leu836=
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ENST00000521107.1:c.321G=
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ENSP00000430161.1:p.Leu107=
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ENST00000522691.1:n.195G=
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|
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ENST00000523756.5:c.4764G=
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|
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NM_003235.4:c.8109G=
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NP_003226.4:p.Leu2703=
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|
XM_005251038.3:c.7917G=
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XP_005251095.1:p.Leu2639=
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XM_006716622.2:c.8046G=
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XP_006716685.1:p.Leu2682=
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XM_005251038.4:c.7917G=
|
XP_005251095.1:p.Leu2639=
|
|
XM_006716622.3:c.8046G=
|
XP_006716685.1:p.Leu2682=
|
|
XM_017013793.1:c.8043G=
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XP_016869282.1:p.Leu2681=
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XM_017013794.1:c.7974G=
|
XP_016869283.1:p.Leu2658=
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|
XM_017013795.1:c.7938G=
|
XP_016869284.1:p.Leu2646=
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XM_017013796.1:c.7890G=
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XP_016869285.1:p.Leu2630=
|
|
XM_017013797.1:c.7848G=
|
XP_016869286.1:p.Leu2616=
|
|
NM_003235.5:c.8109G=
MANE Select
|
NP_003226.4:p.Leu2703=
|
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