ENST00000220616.9:c.8151C=
MANE Select
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ENSP00000220616.4:p.Phe2717=
|
|
ENST00000220616.8:c.8151C=
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ENSP00000220616.4:p.Phe2717=
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|
ENST00000519178.5:c.3517C=
|
|
|
ENST00000519543.5:c.2550C=
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ENSP00000430430.1:p.Phe850=
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|
ENST00000521107.1:c.363C=
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ENSP00000430161.1:p.Phe121=
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|
ENST00000522691.1:n.237C=
|
|
|
ENST00000523756.5:c.4806C=
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|
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NM_003235.4:c.8151C=
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NP_003226.4:p.Phe2717=
|
|
XM_005251038.3:c.7959C=
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XP_005251095.1:p.Phe2653=
|
|
XM_006716622.2:c.8088C=
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XP_006716685.1:p.Phe2696=
|
|
XM_005251038.4:c.7959C=
|
XP_005251095.1:p.Phe2653=
|
|
XM_006716622.3:c.8088C=
|
XP_006716685.1:p.Phe2696=
|
|
XM_017013793.1:c.8085C=
|
XP_016869282.1:p.Phe2695=
|
|
XM_017013794.1:c.8016C=
|
XP_016869283.1:p.Phe2672=
|
|
XM_017013795.1:c.7980C=
|
XP_016869284.1:p.Phe2660=
|
|
XM_017013796.1:c.7932C=
|
XP_016869285.1:p.Phe2644=
|
|
XM_017013797.1:c.7890C=
|
XP_016869286.1:p.Phe2630=
|
|
NM_003235.5:c.8151C=
MANE Select
|
NP_003226.4:p.Phe2717=
|
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