ENST00000261304.7:c.852T>G
MANE Select
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ENSP00000261304.2:p.Gly284=
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ENST00000261304.6:c.852T>G
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ENSP00000261304.2:p.Gly284=
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ENST00000393568.8:c.783T>G
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ENSP00000377198.4:p.Gly261=
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ENST00000393569.6:c.774T>G
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ENSP00000377199.2:p.Gly258=
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ENST00000474294.6:n.842T>G
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ENST00000544807.6:c.684T>G
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ENSP00000437513.2:p.Gly228=
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ENST00000555000.5:c.219T>G
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ENSP00000450472.1:p.Gly73=
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ENST00000557316.5:c.*250T>G
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ENSP00000452314.1:n.*250T>G
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ENST00000622264.4:c.842T>G
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NM_000153.3:c.852T>G
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NP_000144.2:p.Gly284=
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NM_001201401.1:c.783T>G
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NP_001188330.1:p.Gly261=
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NM_001201402.1:c.774T>G
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NP_001188331.1:p.Gly258=
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XM_011536618.1:c.684T>G
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XP_011534920.1:p.Gly228=
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XM_011536618.2:c.684T>G
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XP_011534920.1:p.Gly228=
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NM_000153.4:c.852T>G
MANE Select
|
NP_000144.2:p.Gly284=
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NM_001201401.2:c.783T>G
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NP_001188330.1:p.Gly261=
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NM_001201402.2:c.774T>G
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NP_001188331.1:p.Gly258=
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