ENST00000324041.6:c.475G>T
MANE Select
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ENSP00000326159.1:p.Gly159Cys
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ENST00000324041.5:c.475G>T
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ENSP00000326159.1:p.Gly159Cys
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ENST00000431178.2:c.328G>T
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ENSP00000399448.2:p.Gly110Trp
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ENST00000593885.1:c.190G>T
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ENSP00000469769.1:p.Glu64Ter
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ENST00000596876.1:n.394G>T
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ENST00000598305.5:c.190G>T
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ENSP00000469963.1:p.Glu64Ter
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ENST00000599865.5:n.328G>T
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ENST00000602148.1:c.487G>T
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ENSP00000472091.1:n.487G>T
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NM_001302961.1:c.190G>T
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NP_001289890.1:p.Gly64Cys
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NM_004917.4:c.475G>T
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NP_004908.4:p.Gly159Cys
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NR_126566.1:n.468G>T
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XM_005259441.3:c.190G>T
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XP_005259498.2:p.Gly64Cys
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XM_011527545.1:c.475G>T
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XP_011525847.1:p.Glu159Ter
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XM_011527546.1:c.475G>T
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XP_011525848.1:p.Gly159Trp
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XM_011527547.1:c.328G>T
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XP_011525849.1:p.Gly110Cys
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XM_005259441.4:c.190G>T
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XP_005259498.2:p.Gly64Cys
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XM_011527545.3:c.475G>T
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XP_011525847.1:p.Glu159Ter
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XM_011527546.2:c.475G>T
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XP_011525848.1:p.Gly159Trp
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NM_001302961.2:c.190G>T
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NP_001289890.1:p.Gly64Cys
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NR_126566.2:n.468G>T
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NM_004917.5:c.475G>T
MANE Select
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NP_004908.4:p.Gly159Cys
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