ENST00000367698.4:c.886G>T
MANE Select
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ENSP00000356671.3:p.Ala296Ser
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ENST00000367698.3:c.886G>T
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ENSP00000356671.3:p.Ala296Ser
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ENST00000487183.1:n.537G>T
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|
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ENST00000617423.4:c.559+2045G>T
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ENSP00000478688.1:n.559+2045G>T
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NM_000488.3:c.886G>T , LRG_577t1:c.886G>T
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NP_000479.1:p.Ala296Ser
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XM_005245198.2:c.742G>T
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XP_005245255.1:p.Ala248Ser
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NM_001365052.1:c.742G>T
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NP_001351981.1:p.Ala248Ser
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NM_000488.4:c.886G>T
MANE Select
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NP_000479.1:p.Ala296Ser
|
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NM_001365052.2:c.742G>T
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NP_001351981.1:p.Ala248Ser
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NM_001386302.1:c.1009G>T
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NP_001373231.1:p.Ala337Ser
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NM_001386303.1:c.967G>T
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NP_001373232.1:p.Ala323Ser
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NM_001386304.1:c.865G>T
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NP_001373233.1:p.Ala289Ser
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NM_001386305.1:c.829G>T
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NP_001373234.1:p.Ala277Ser
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NM_001386306.1:c.670G>T
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NP_001373235.1:p.Ala224Ser
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