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ENST00000641023.2:c.486C=
MANE Select
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ENST00000641074.1:c.486C=
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ENSP00000493446.1:p.Thr162=
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NM_006623.3:c.486C=
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XM_011541226.1:c.708C=
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XP_011539528.1:p.Thr236=
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XP_011539532.1:p.Thr67=
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XM_011541226.2:c.708C=
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XP_011539529.1:p.Thr210=
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XM_011541228.2:c.597C=
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XM_011541231.2:c.192C=
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XP_011539533.1:p.Thr64=
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XM_024446338.1:c.597C=
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XP_024302106.1:p.Thr199=
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NM_006623.4:c.486C=
MANE Select
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NP_006614.2:p.Thr162=
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