ENST00000217260.9:c.212A=
MANE Select
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ENSP00000217260.4:p.His71=
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ENST00000217260.8:c.212A=
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ENSP00000217260.4:p.His71=
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ENST00000400634.2:c.212A=
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ENSP00000383475.2:p.His71=
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NM_001029871.3:c.212A=
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NP_001025042.2:p.His71=
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NM_001040007.2:c.212A=
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NP_001035096.1:p.His71=
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XM_011529232.1:c.260A=
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XP_011527534.1:p.His87=
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XM_011529233.1:c.260A=
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XP_011527535.1:p.His87=
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XR_937068.1:n.332A=
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XR_937069.1:n.327A=
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XM_017027839.1:c.212A=
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XP_016883328.1:p.His71=
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NM_001029871.4:c.212A=
MANE Select
|
NP_001025042.2:p.His71=
|
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NM_001040007.3:c.212A=
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NP_001035096.1:p.His71=
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