ENST00000399503.4:c.2702C=
MANE Select
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ENSP00000382423.3:p.Ser901=
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ENST00000399503.3:c.2702C=
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ENSP00000382423.3:p.Ser901=
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NM_005921.1:c.2702C=
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NP_005912.1:p.Ser901=
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XM_005248519.3:c.2324C=
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XP_005248576.2:p.Ser775=
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XM_011543406.1:c.2447C=
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XP_011541708.1:p.Ser816=
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XM_011543407.1:c.2423C=
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XP_011541709.1:p.Ser808=
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XM_011543408.1:c.2702C=
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XP_011541710.1:p.Ser901=
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XM_017009484.1:c.2291C=
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XP_016864973.1:p.Ser764=
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XM_017009485.1:c.2213C=
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XP_016864974.1:p.Ser738=
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XR_001742068.2:n.2733C=
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|
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NM_005921.2:c.2702C=
MANE Select
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NP_005912.1:p.Ser901=
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