ENST00000367698.4:c.1232G>T
MANE Select
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ENSP00000356671.3:p.Gly411Val
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ENST00000367698.3:c.1232G>T
|
ENSP00000356671.3:p.Gly411Val
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ENST00000617423.4:c.617G>T
|
ENSP00000478688.1:p.Gly206Val
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NM_000488.3:c.1232G>T , LRG_577t1:c.1232G>T
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NP_000479.1:p.Gly411Val
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XM_005245198.2:c.1088G>T
|
XP_005245255.1:p.Gly363Val
|
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NM_001365052.1:c.1088G>T
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NP_001351981.1:p.Gly363Val
|
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NM_000488.4:c.1232G>T
MANE Select
|
NP_000479.1:p.Gly411Val
|
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NM_001365052.2:c.1088G>T
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NP_001351981.1:p.Gly363Val
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NM_001386302.1:c.1355G>T
|
NP_001373231.1:p.Gly452Val
|
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NM_001386303.1:c.1313G>T
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NP_001373232.1:p.Gly438Val
|
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NM_001386304.1:c.1211G>T
|
NP_001373233.1:p.Gly404Val
|
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NM_001386305.1:c.1175G>T
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NP_001373234.1:p.Gly392Val
|
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NM_001386306.1:c.1016G>T
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NP_001373235.1:p.Gly339Val
|
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