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ENSP00000453157.3:p.His203=
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ENSP00000514528.1:n.*97T=
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ENST00000267415.12:c.717T=
MANE Select
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ENSP00000453157.2:p.His203=
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XP_005267585.1:p.His239=
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XP_005267586.1:p.His204=
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NM_001099274.2:c.717T=
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NP_001092744.1:p.His239=
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NM_001363668.1:c.612T=
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NP_001350597.1:p.His204=
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NM_012461.3:c.717T=
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NP_036593.2:p.His239=
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XM_011536642.2:c.*97T=
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XP_011534944.1:n.*97T=
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XM_017021217.1:c.75T=
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XP_016876706.1:p.His25=
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NM_001099274.3:c.717T=
MANE Select
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NP_001092744.1:p.His239=
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NM_001363668.2:c.612T=
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NP_001350597.1:p.His204=
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