ENST00000268695.10:c.870C>G
MANE Select
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ENSP00000268695.5:p.Gly290=
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|
ENST00000268695.9:c.870C>G
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ENSP00000268695.5:p.Gly290=
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|
ENST00000562593.5:n.4279C>G
|
|
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ENST00000562931.5:n.458C>G
|
|
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ENST00000567525.5:c.551C>G
|
ENSP00000454484.1:n.551C>G
|
|
ENST00000568613.5:c.989C>G
|
ENSP00000457921.1:n.989C>G
|
|
NM_000512.4:c.870C>G
|
NP_000503.1:p.Gly290=
|
|
XM_005256301.2:c.870C>G
|
XP_005256358.1:p.Gly290=
|
|
XM_005256302.1:c.888C>G
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XP_005256359.1:p.Gly296=
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|
XM_011522982.1:c.888C>G
|
XP_011521284.1:p.Gly296=
|
|
XM_011522984.1:c.888C>G
|
XP_011521286.1:p.Gly296=
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NM_001323543.1:c.315C>G
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NP_001310472.1:p.Gly105=
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|
NM_001323544.1:c.888C>G
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NP_001310473.1:p.Gly296=
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|
XM_005256301.3:c.870C>G
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XP_005256358.1:p.Gly290=
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|
XM_011522982.2:c.888C>G
|
XP_011521284.1:p.Gly296=
|
|
XM_017023111.2:c.888C>G
|
XP_016878600.1:p.Gly296=
|
|
XM_017023112.2:c.888C>G
|
XP_016878601.1:p.Gly296=
|
|
XM_017023113.1:c.315C>G
|
XP_016878602.1:p.Gly105=
|
|
NM_000512.5:c.870C>G
MANE Select
|
NP_000503.1:p.Gly290=
|
|
NM_001323543.2:c.315C>G
|
NP_001310472.1:p.Gly105=
|
|
NM_001323544.2:c.888C>G
|
NP_001310473.1:p.Gly296=
|
|