ENST00000265713.8:c.4412T>G
MANE Select
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ENSP00000265713.2:p.Val1471Gly
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ENST00000396930.4:c.4412T>G
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ENSP00000380136.3:p.Val1471Gly
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ENST00000406337.6:c.4418T>G
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ENSP00000385888.2:p.Val1473Gly
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ENST00000648335.1:c.4412T>G
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ENSP00000497086.1:p.Val1471Gly
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ENST00000649817.1:c.3093T>G
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ENST00000265713.6:c.4412T>G
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ENSP00000265713.2:p.Val1471Gly
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ENST00000396930.3:c.4412T>G
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ENSP00000380136.3:p.Val1471Gly
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ENST00000406337.5:c.4412T>G
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ENSP00000385888.1:p.Val1471Gly
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NM_001099412.1:c.4412T>G
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NP_001092882.1:p.Val1471Gly
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NM_001099413.1:c.4412T>G
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NP_001092883.1:p.Val1471Gly
|
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NM_006766.3:c.4412T>G
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NP_006757.2:p.Val1471Gly
|
|
NM_006766.4:c.4412T>G
|
NP_006757.2:p.Val1471Gly
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XM_011544656.1:c.4544T>G
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XP_011542958.1:p.Val1515Gly
|
|
XM_011544657.1:c.4544T>G
|
XP_011542959.1:p.Val1515Gly
|
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XM_011544658.1:c.4544T>G
|
XP_011542960.1:p.Val1515Gly
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|
XM_011544659.1:c.4523T>G
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XP_011542961.1:p.Val1508Gly
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XM_011544660.1:c.4430T>G
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XP_011542962.1:p.Val1477Gly
|
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XM_011544656.2:c.4544T>G
|
XP_011542958.1:p.Val1515Gly
|
|
XM_011544657.3:c.4544T>G
|
XP_011542959.1:p.Val1515Gly
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|
XM_011544658.3:c.4544T>G
|
XP_011542960.1:p.Val1515Gly
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|
XM_011544659.2:c.4523T>G
|
XP_011542961.1:p.Val1508Gly
|
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XM_017013863.1:c.4412T>G
|
XP_016869352.1:p.Val1471Gly
|
|
XM_017013864.2:c.4412T>G
|
XP_016869353.1:p.Val1471Gly
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XM_024447285.1:c.2984T>G
|
XP_024303053.1:p.Val995Gly
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NM_006766.5:c.4412T>G
MANE Select
|
NP_006757.2:p.Val1471Gly
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