ENST00000367698.4:c.1393T>G
MANE Select
|
ENSP00000356671.3:p.Ter465Glu
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ENST00000367698.3:c.1393T>G
|
ENSP00000356671.3:p.Ter465Glu
|
|
ENST00000617423.4:c.778T>G
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ENSP00000478688.1:p.Ter260Glu
|
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NM_000488.3:c.1393T>G , LRG_577t1:c.1393T>G
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NP_000479.1:p.Ter465Glu
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XM_005245198.2:c.1249T>G
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XP_005245255.1:p.Ter417Glu
|
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NM_001365052.1:c.1249T>G
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NP_001351981.1:p.Ter417Glu
|
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NM_000488.4:c.1393T>G
MANE Select
|
NP_000479.1:p.Ter465Glu
|
|
NM_001365052.2:c.1249T>G
|
NP_001351981.1:p.Ter417Glu
|
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NM_001386302.1:c.1516T>G
|
NP_001373231.1:p.Ter506Glu
|
|
NM_001386303.1:c.1474T>G
|
NP_001373232.1:p.Ter492Glu
|
|
NM_001386304.1:c.1372T>G
|
NP_001373233.1:p.Ter458Glu
|
|
NM_001386305.1:c.1336T>G
|
NP_001373234.1:p.Ter446Glu
|
|
NM_001386306.1:c.1177T>G
|
NP_001373235.1:p.Ter393Glu
|
|