ENST00000029410.10:c.346C=
MANE Select
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ENSP00000029410.5:p.Arg116=
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ENST00000029410.9:c.346C=
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ENSP00000029410.5:p.Arg116=
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ENST00000502420.1:n.325C=
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ENST00000505433.5:c.346C=
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ENSP00000425591.1:p.Arg116=
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ENST00000505468.1:c.4C=
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ENSP00000420886.1:p.Arg2=
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ENST00000507061.1:c.163C=
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ENSP00000423868.1:p.Arg55=
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ENST00000510761.1:c.4C=
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ENSP00000423438.1:p.Arg2=
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NM_007255.2:c.346C=
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NP_009186.1:p.Arg116=
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XM_005265805.2:c.4C=
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XP_005265862.1:p.Arg2=
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XM_006714816.2:c.-154C=
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XP_006714879.1:n.-154C=
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XM_011534421.1:c.4C=
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XP_011532723.1:p.Arg2=
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XM_006714816.4:c.-154C=
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XP_006714879.1:n.-154C=
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XM_017008999.2:c.4C=
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XP_016864488.1:p.Arg2=
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NM_007255.3:c.346C=
MANE Select
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NP_009186.1:p.Arg116=
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