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ENSP00000507057.1:n.2186-8223C=
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ENST00000382292.9:c.13009C=
MANE Select
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ENSP00000390925.2:n.2186-1383C=
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NM_014363.5:c.13009C=
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XM_005266338.2:c.13036C=
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XP_005266395.1:p.His4346=
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XM_011535039.2:c.13027C=
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XP_011533341.1:p.His4343=
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XM_017020539.1:c.13000C=
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XM_024449337.1:c.13036C=
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XP_024305105.1:p.His4346=
|
|
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NM_014363.6:c.13009C=
MANE Select
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NP_055178.3:p.His4337=
|
|
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NM_001278055.2:c.12568C=
|
NP_001264984.1:p.His4190=
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