ENST00000328381.10:c.772G>A
MANE Select
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ENSP00000328340.5:p.Ala258Thr
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ENST00000324689.8:c.609G>A
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ENSP00000323693.4:p.Gly203=
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ENST00000328381.9:c.772G>A
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ENSP00000328340.5:p.Ala258Thr
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ENST00000443677.6:c.465G>A
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ENSP00000411965.2:p.Gly155=
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ENST00000535306.6:c.837G>A
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ENSP00000440470.2:p.Gly279=
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NM_001184992.1:c.837G>A
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NP_001171921.1:p.Gly279=
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NM_032322.3:c.772G>A
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NP_115698.3:p.Ala258Thr
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NM_197939.1:c.609G>A
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NP_922921.1:p.Gly203=
|
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XM_005258043.3:c.229G>A
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XP_005258100.1:p.Ala77Thr
|
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XM_006722138.2:c.451G>A
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XP_006722201.1:p.Ala151Thr
|
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XM_017025223.1:c.229G>A
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XP_016880712.1:p.Ala77Thr
|
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XM_024451000.1:c.229G>A
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XP_024306768.1:p.Ala77Thr
|
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XM_024451001.1:c.229G>A
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XP_024306769.1:p.Ala77Thr
|
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XR_002958076.1:n.1105G>A
|
|
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XR_002958077.1:n.1040G>A
|
|
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XR_002958078.1:n.877G>A
|
|
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NM_032322.4:c.772G>A
MANE Select
|
NP_115698.3:p.Ala258Thr
|
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NM_001184992.2:c.837G>A
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NP_001171921.1:p.Gly279=
|
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NM_197939.2:c.609G>A
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NP_922921.1:p.Gly203=
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