ENST00000324041.6:c.524A>G
MANE Select
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ENSP00000326159.1:p.Glu175Gly
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ENST00000324041.5:c.524A>G
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ENSP00000326159.1:p.Glu175Gly
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|
ENST00000431178.2:c.328+132A>G
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ENSP00000399448.2:n.328+132A>G
|
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ENST00000593885.1:c.*19A>G
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ENSP00000469769.1:n.*19A>G
|
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ENST00000596876.1:n.526A>G
|
|
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ENST00000598305.5:c.*19A>G
|
ENSP00000469963.1:n.*19A>G
|
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ENST00000599865.5:n.460A>G
|
|
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ENST00000602148.1:c.536A>G
|
ENSP00000472091.1:n.536A>G
|
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NM_001302961.1:c.239A>G
|
NP_001289890.1:p.Glu80Gly
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NM_004917.4:c.524A>G
|
NP_004908.4:p.Glu175Gly
|
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NR_126566.1:n.513A>G
|
|
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XM_005259441.3:c.239A>G
|
XP_005259498.2:p.Glu80Gly
|
|
XM_011527545.1:c.*19A>G
|
XP_011525847.1:n.*19A>G
|
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XM_011527546.1:c.475+132A>G
|
XP_011525848.1:n.475+132A>G
|
|
XM_011527547.1:c.377A>G
|
XP_011525849.1:p.Glu126Gly
|
|
XM_005259441.4:c.239A>G
|
XP_005259498.2:p.Glu80Gly
|
|
XM_011527545.3:c.*19A>G
|
XP_011525847.1:n.*19A>G
|
|
XM_011527546.2:c.475+132A>G
|
XP_011525848.1:n.475+132A>G
|
|
NM_001302961.2:c.239A>G
|
NP_001289890.1:p.Glu80Gly
|
|
NR_126566.2:n.513A>G
|
|
|
NM_004917.5:c.524A>G
MANE Select
|
NP_004908.4:p.Glu175Gly
|
|