ENST00000311106.8:c.285+109G>T
MANE Select
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ENSP00000308024.2:n.285+109G>T
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ENST00000311106.7:c.285+109G>T
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ENSP00000308024.2:n.285+109G>T
|
|
ENST00000508626.5:c.144+109G>T
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ENSP00000421600.1:n.144+109G>T
|
|
ENST00000509190.1:c.285+109G>T
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ENSP00000427294.1:n.285+109G>T
|
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NM_000439.4:c.285+109G>T
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NP_000430.3:n.285+109G>T
|
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NM_001177875.1:c.144+109G>T
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NP_001171346.1:n.144+109G>T
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|
NR_130776.1:n.354+49452C>A
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|
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NM_000439.5:c.285+109G>T
MANE Select
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NP_000430.3:n.285+109G>T
|
|
NM_001177875.2:c.144+109G>T
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NP_001171346.1:n.144+109G>T
|
|