ENST00000220616.9:c.8178G=
MANE Select
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ENSP00000220616.4:p.Lys2726=
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|
ENST00000220616.8:c.8178G=
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ENSP00000220616.4:p.Lys2726=
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|
ENST00000519178.5:c.3544G=
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|
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ENST00000519543.5:c.2577G=
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ENSP00000430430.1:p.Lys859=
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|
ENST00000521107.1:c.390G=
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ENSP00000430161.1:p.Lys130=
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|
ENST00000522691.1:n.264G=
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|
|
ENST00000523756.5:c.4833G=
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|
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NM_003235.4:c.8178G=
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NP_003226.4:p.Lys2726=
|
|
XM_005251038.3:c.7986G=
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XP_005251095.1:p.Lys2662=
|
|
XM_006716622.2:c.8115G=
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XP_006716685.1:p.Lys2705=
|
|
XM_005251038.4:c.7986G=
|
XP_005251095.1:p.Lys2662=
|
|
XM_006716622.3:c.8115G=
|
XP_006716685.1:p.Lys2705=
|
|
XM_017013793.1:c.8112G=
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XP_016869282.1:p.Lys2704=
|
|
XM_017013794.1:c.8043G=
|
XP_016869283.1:p.Lys2681=
|
|
XM_017013795.1:c.8007G=
|
XP_016869284.1:p.Lys2669=
|
|
XM_017013796.1:c.7959G=
|
XP_016869285.1:p.Lys2653=
|
|
XM_017013797.1:c.7917G=
|
XP_016869286.1:p.Lys2639=
|
|
NM_003235.5:c.8178G=
MANE Select
|
NP_003226.4:p.Lys2726=
|
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