ENST00000367698.4:c.1078G>T
MANE Select
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ENSP00000356671.3:p.Gly360Cys
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ENST00000367698.3:c.1078G>T
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ENSP00000356671.3:p.Gly360Cys
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ENST00000617423.4:c.560-2134G>T
|
ENSP00000478688.1:n.560-2134G>T
|
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NM_000488.3:c.1078G>T , LRG_577t1:c.1078G>T
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NP_000479.1:p.Gly360Cys
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XM_005245198.2:c.934G>T
|
XP_005245255.1:p.Gly312Cys
|
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NM_001365052.1:c.934G>T
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NP_001351981.1:p.Gly312Cys
|
|
NM_000488.4:c.1078G>T
MANE Select
|
NP_000479.1:p.Gly360Cys
|
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NM_001365052.2:c.934G>T
|
NP_001351981.1:p.Gly312Cys
|
|
NM_001386302.1:c.1201G>T
|
NP_001373231.1:p.Gly401Cys
|
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NM_001386303.1:c.1159G>T
|
NP_001373232.1:p.Gly387Cys
|
|
NM_001386304.1:c.1057G>T
|
NP_001373233.1:p.Gly353Cys
|
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NM_001386305.1:c.1021G>T
|
NP_001373234.1:p.Gly341Cys
|
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NM_001386306.1:c.862G>T
|
NP_001373235.1:p.Gly288Cys
|
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