ENST00000220616.9:c.8183C=
MANE Select
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ENSP00000220616.4:p.Ser2728=
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ENST00000220616.8:c.8183C=
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ENSP00000220616.4:p.Ser2728=
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|
ENST00000519178.5:c.3549C=
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|
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ENST00000519543.5:c.2582C=
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ENSP00000430430.1:p.Ser861=
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ENST00000521107.1:c.395C=
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ENSP00000430161.1:p.Ser132=
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ENST00000522691.1:n.269C=
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|
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ENST00000523756.5:c.4838C=
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|
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NM_003235.4:c.8183C=
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NP_003226.4:p.Ser2728=
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XM_005251038.3:c.7991C=
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XP_005251095.1:p.Ser2664=
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XM_006716622.2:c.8120C=
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XP_006716685.1:p.Ser2707=
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XM_005251038.4:c.7991C=
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XP_005251095.1:p.Ser2664=
|
|
XM_006716622.3:c.8120C=
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XP_006716685.1:p.Ser2707=
|
|
XM_017013793.1:c.8117C=
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XP_016869282.1:p.Ser2706=
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XM_017013794.1:c.8048C=
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XP_016869283.1:p.Ser2683=
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XM_017013795.1:c.8012C=
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XP_016869284.1:p.Ser2671=
|
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XM_017013796.1:c.7964C=
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XP_016869285.1:p.Ser2655=
|
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XM_017013797.1:c.7922C=
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XP_016869286.1:p.Ser2641=
|
|
NM_003235.5:c.8183C=
MANE Select
|
NP_003226.4:p.Ser2728=
|
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