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ENST00000205557.12:c.3661C=
MANE Select
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ENST00000640696.1:c.475C=
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ENSP00000492197.1:p.Arg159=
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ENST00000622290.4:c.*870C=
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ENSP00000483331.1:n.*870C=
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NM_001171.5:c.3661C=
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NP_001162.4:p.Arg1221=
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XM_011522479.1:c.3628C=
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XP_011520781.1:p.Arg1210=
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XP_011520782.1:p.Arg1107=
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XM_011522481.1:c.3319C=
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XR_932837.1:n.3697C=
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XR_932838.1:n.3697C=
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XR_933134.1:n.539-225G=
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NM_001351800.1:c.3319C=
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NP_001338729.1:p.Arg1107=
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XP_011520781.1:p.Arg1210=
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XM_011522481.3:c.3319C=
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XP_016878701.1:p.Arg1165=
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XR_932838.3:n.3642C=
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NM_001171.6:c.3661C=
MANE Select
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NP_001162.5:p.Arg1221=
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