ENST00000260408.8:c.516C>G
MANE Select
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ENSP00000260408.3:p.Gly172=
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ENST00000260408.7:c.516C>G
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ENSP00000260408.3:p.Gly172=
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ENST00000396136.6:c.342C>G
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ENST00000402627.5:c.56-24336C>G
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ENSP00000386056.1:n.56-24336C>G
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ENST00000439637.5:c.357C>G
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ENSP00000391930.1:p.Gly119=
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ENST00000497846.5:n.633C>G
|
|
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ENST00000558733.5:n.752C>G
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ENST00000559053.1:c.56-24336C>G
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ENSP00000453952.1:n.56-24336C>G
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ENST00000561288.1:c.56-67648C>G
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ENSP00000452639.1:n.56-67648C>G
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NM_001110.3:c.516C>G
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NP_001101.1:p.Gly172=
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XM_005254117.2:c.516C>G
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XP_005254174.1:p.Gly172=
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NM_001320570.1:c.516C>G
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NP_001307499.1:p.Gly172=
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XM_024449818.1:c.294C>G
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XP_024305586.1:p.Gly98=
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NM_001110.4:c.516C>G
MANE Select
|
NP_001101.1:p.Gly172=
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NM_001320570.2:c.516C>G
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NP_001307499.1:p.Gly172=
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