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ENST00000642864.1:c.762T=
MANE Select
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ENSP00000495726.1:p.Ser254=
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ENST00000674510.1:c.762T=
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ENSP00000502054.1:p.Ser254=
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NM_001111125.2:c.762T=
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NP_001104595.1:p.Ser254=
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NM_015075.1:c.147T=
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NP_055890.1:p.Ser49=
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XM_006724579.2:c.858T=
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XP_006724642.1:p.Ser286=
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XP_011529076.1:p.Ser286=
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XP_011529079.1:p.Ser286=
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XP_006724645.1:p.Ser286=
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XM_006724583.4:c.858T=
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XP_006724646.1:p.Ser286=
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XM_006724584.3:c.858T=
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XP_006724647.1:p.Ser286=
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XM_011530773.2:c.51T=
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XP_011529076.1:p.Ser286=
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XM_011530776.2:c.858T=
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XP_011529078.1:p.Ser286=
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XM_011530777.2:c.858T=
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XP_011529079.1:p.Ser286=
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XM_017029359.2:c.732T=
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XP_016884849.1:p.Ser88=
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XR_938365.2:n.1079T=
|
|
|
NM_001111125.3:c.762T=
MANE Select
|
NP_001104595.1:p.Ser254=
|
|
NM_015075.2:c.147T=
|
NP_055890.1:p.Ser49=
|
|