ENST00000328300.11:c.4786T=
MANE Select
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ENSP00000331902.7:p.Trp1596=
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ENST00000361603.7:c.4768T=
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ENSP00000354505.2:p.Trp1590=
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ENST00000510690.2:n.1280T=
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ENST00000644079.1:n.1272T=
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ENST00000328300.10:c.4786T=
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ENSP00000331902.6:p.Trp1596=
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ENST00000361603.6:c.4768T=
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ENSP00000354505.2:p.Trp1590=
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ENST00000504541.1:c.184T=
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ENSP00000424845.1:p.Trp62=
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ENST00000515658.1:c.325-1411T=
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NM_000495.4:c.4768T=
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NP_000486.1:p.Trp1590=
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NM_033380.2:c.4786T=
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NP_203699.1:p.Trp1596=
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XM_005262070.2:c.4777T=
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XP_005262127.1:p.Trp1593=
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XM_006724616.2:c.4786T=
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XP_006724679.1:p.Trp1596=
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XM_011530849.1:c.4462T=
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XP_011529151.1:p.Trp1488=
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XM_011530851.1:c.2359T=
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XP_011529153.1:p.Trp787=
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XM_011530849.2:c.4801T=
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XP_011529151.2:p.Trp1601=
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XM_017029259.2:c.4792T=
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XP_016884748.1:p.Trp1598=
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XM_017029260.1:c.4783T=
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XP_016884749.1:p.Trp1595=
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XM_017029263.2:c.3121T=
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XP_016884752.1:p.Trp1041=
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NM_000495.5:c.4768T=
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NP_000486.1:p.Trp1590=
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NM_033380.3:c.4786T=
MANE Select
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NP_203699.1:p.Trp1596=
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