ENST00000377636.8:c.2593+51A>G
MANE Select
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ENSP00000366863.3:n.2593+51A>G
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ENST00000648194.1:c.1861+51A>G
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ENSP00000496983.1:n.1861+51A>G
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|
ENST00000377625.6:c.2404+51A>G
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ENSP00000366852.2:n.2404+51A>G
|
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ENST00000377636.7:c.2593+51A>G
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ENSP00000366863.3:n.2593+51A>G
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ENST00000431480.6:c.2569+51A>G
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ENSP00000395986.2:n.2569+51A>G
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ENST00000493487.1:n.452+51A>G
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|
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NM_001286658.1:c.2569+51A>G
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NP_001273587.1:n.2569+51A>G
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NM_001286658.2:c.2569+51A>G
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NP_001273587.1:n.2569+51A>G
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|
NM_001286659.1:c.2404+51A>G
|
NP_001273588.1:n.2404+51A>G
|
|
NM_001286659.2:c.2404+51A>G
|
NP_001273588.1:n.2404+51A>G
|
|
NM_014832.3:c.2593+51A>G
|
NP_055647.2:n.2593+51A>G
|
|
NM_014832.4:c.2593+51A>G
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NP_055647.2:n.2593+51A>G
|
|
XM_005266603.1:c.2518+51A>G
|
XP_005266660.1:n.2518+51A>G
|
|
XM_005266605.1:c.2050+51A>G
|
XP_005266662.1:n.2050+51A>G
|
|
XM_006719903.2:c.2119+51A>G
|
XP_006719966.1:n.2119+51A>G
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|
XM_011535331.1:c.2482+51A>G
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XP_011533633.1:n.2482+51A>G
|
|
XM_005266603.2:c.2518+51A>G
|
XP_005266660.1:n.2518+51A>G
|
|
XM_005266605.3:c.2050+51A>G
|
XP_005266662.1:n.2050+51A>G
|
|
XM_006719903.3:c.2119+51A>G
|
XP_006719966.1:n.2119+51A>G
|
|
XM_011535331.2:c.2482+51A>G
|
XP_011533633.1:n.2482+51A>G
|
|
XM_017020882.2:c.1861+51A>G
|
XP_016876371.1:n.1861+51A>G
|
|
XM_017020883.2:c.1750+51A>G
|
XP_016876372.1:n.1750+51A>G
|
|
XM_017020884.2:c.160+51A>G
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XP_016876373.1:n.160+51A>G
|
|
NM_014832.5:c.2593+51A>G
MANE Select
|
NP_055647.2:n.2593+51A>G
|
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