ENST00000268695.10:c.843C=
MANE Select
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ENSP00000268695.5:p.Thr281=
|
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ENST00000268695.9:c.843C=
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ENSP00000268695.5:p.Thr281=
|
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ENST00000562593.5:n.4252C=
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|
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ENST00000562931.5:n.431C=
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|
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ENST00000567525.5:c.524C=
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ENSP00000454484.1:n.524C=
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|
ENST00000568613.5:c.962C=
|
ENSP00000457921.1:n.962C=
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|
NM_000512.4:c.843C=
|
NP_000503.1:p.Thr281=
|
|
XM_005256301.2:c.843C=
|
XP_005256358.1:p.Thr281=
|
|
XM_005256302.1:c.861C=
|
XP_005256359.1:p.Thr287=
|
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XM_011522982.1:c.861C=
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XP_011521284.1:p.Thr287=
|
|
XM_011522984.1:c.861C=
|
XP_011521286.1:p.Thr287=
|
|
NM_001323543.1:c.288C=
|
NP_001310472.1:p.Thr96=
|
|
NM_001323544.1:c.861C=
|
NP_001310473.1:p.Thr287=
|
|
XM_005256301.3:c.843C=
|
XP_005256358.1:p.Thr281=
|
|
XM_011522982.2:c.861C=
|
XP_011521284.1:p.Thr287=
|
|
XM_017023111.2:c.861C=
|
XP_016878600.1:p.Thr287=
|
|
XM_017023112.2:c.861C=
|
XP_016878601.1:p.Thr287=
|
|
XM_017023113.1:c.288C=
|
XP_016878602.1:p.Thr96=
|
|
NM_000512.5:c.843C=
MANE Select
|
NP_000503.1:p.Thr281=
|
|
NM_001323543.2:c.288C=
|
NP_001310472.1:p.Thr96=
|
|
NM_001323544.2:c.861C=
|
NP_001310473.1:p.Thr287=
|
|