ENST00000374479.4:c.1035_1042delinsACTGATTG
MANE Select
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ENSP00000363603.3:p.Gly345=
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ENST00000374479.3:c.1035_1042delinsACTGATTG
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ENSP00000363603.3:p.Gly345=
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NM_000147.4:c.1035_1042delinsACTGATTG
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NP_000138.2:p.Gly345=
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XM_005245821.1:c.660_667delinsACTGATTG
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XP_005245878.1:p.Gly220=
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XM_011541167.1:c.402_409delinsACTGATTG
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XP_011539469.1:p.Gly134=
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XM_005245821.3:c.660_667delinsACTGATTG
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XP_005245878.1:p.Gly220=
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XM_011541167.3:c.402_409delinsACTGATTG
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XP_011539469.1:p.Gly134=
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XM_017000905.2:c.732_739delinsACTGATTG
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XP_016856394.1:p.Gly244=
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NM_000147.5:c.1035_1042delinsACTGATTG
MANE Select
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NP_000138.2:p.Gly345=
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NR_174379.1:n.1213_1220delinsACTGATTG
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NR_174380.1:n.1262_1269delinsACTGATTG
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NR_174381.1:n.1101_1108delinsACTGATTG
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NR_174382.1:n.1498_1505delinsACTGATTG
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