ENST00000266771.10:c.573T=
MANE Select
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ENSP00000266771.5:p.Thr191=
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ENST00000266771.9:c.573T=
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ENSP00000266771.5:p.Thr191=
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ENST00000366292.6:n.885T=
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ENST00000376740.8:c.152T=
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ENST00000376744.8:c.409T=
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ENST00000535272.1:n.367T=
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ENST00000539703.1:n.223T=
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NM_145648.3:c.573T=
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NP_663623.1:p.Thr191=
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XM_011537895.1:c.723T=
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XP_011536197.1:p.Thr241=
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XR_429081.2:n.596T=
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XR_944494.1:n.746T=
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XR_944495.1:n.746T=
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XR_944496.1:n.746T=
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XR_944497.1:n.746T=
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XM_017018791.1:c.723T=
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XP_016874280.1:p.Thr241=
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XM_017018792.1:c.723T=
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XP_016874281.1:p.Thr241=
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XM_017018793.1:c.573T=
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XP_016874282.1:p.Thr191=
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XR_002957287.1:n.596T=
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XR_944496.2:n.746T=
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NM_145648.4:c.573T=
MANE Select
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NP_663623.1:p.Thr191=
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