ENST00000367698.4:c.913C>G
MANE Select
|
ENSP00000356671.3:p.Pro305Ala
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ENST00000367698.3:c.913C>G
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ENSP00000356671.3:p.Pro305Ala
|
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ENST00000487183.1:n.564C>G
|
|
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ENST00000617423.4:c.559+2072C>G
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ENSP00000478688.1:n.559+2072C>G
|
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NM_000488.3:c.913C>G , LRG_577t1:c.913C>G
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NP_000479.1:p.Pro305Ala
|
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XM_005245198.2:c.769C>G
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XP_005245255.1:p.Pro257Ala
|
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NM_001365052.1:c.769C>G
|
NP_001351981.1:p.Pro257Ala
|
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NM_000488.4:c.913C>G
MANE Select
|
NP_000479.1:p.Pro305Ala
|
|
NM_001365052.2:c.769C>G
|
NP_001351981.1:p.Pro257Ala
|
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NM_001386302.1:c.1036C>G
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NP_001373231.1:p.Pro346Ala
|
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NM_001386303.1:c.994C>G
|
NP_001373232.1:p.Pro332Ala
|
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NM_001386304.1:c.892C>G
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NP_001373233.1:p.Pro298Ala
|
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NM_001386305.1:c.856C>G
|
NP_001373234.1:p.Pro286Ala
|
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NM_001386306.1:c.697C>G
|
NP_001373235.1:p.Pro233Ala
|
|