ENST00000367698.4:c.1104A>C
MANE Select
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ENSP00000356671.3:p.Gln368His
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ENST00000367698.3:c.1104A>C
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ENSP00000356671.3:p.Gln368His
|
|
ENST00000617423.4:c.560-2108A>C
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ENSP00000478688.1:n.560-2108A>C
|
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NM_000488.3:c.1104A>C , LRG_577t1:c.1104A>C
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NP_000479.1:p.Gln368His
|
|
XM_005245198.2:c.960A>C
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XP_005245255.1:p.Gln320His
|
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NM_001365052.1:c.960A>C
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NP_001351981.1:p.Gln320His
|
|
NM_000488.4:c.1104A>C
MANE Select
|
NP_000479.1:p.Gln368His
|
|
NM_001365052.2:c.960A>C
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NP_001351981.1:p.Gln320His
|
|
NM_001386302.1:c.1227A>C
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NP_001373231.1:p.Gln409His
|
|
NM_001386303.1:c.1185A>C
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NP_001373232.1:p.Gln395His
|
|
NM_001386304.1:c.1083A>C
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NP_001373233.1:p.Gln361His
|
|
NM_001386305.1:c.1047A>C
|
NP_001373234.1:p.Gln349His
|
|
NM_001386306.1:c.888A>C
|
NP_001373235.1:p.Gln296His
|
|