ENST00000382080.6:c.39+167693A>T
MANE Select
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ENSP00000371512.1:n.39+167693A>T
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ENST00000382080.5:c.39+167693A>T
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ENSP00000371512.1:n.39+167693A>T
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NM_139167.2:c.39+167693A>T , LRG_208t1:c.39+167693A>T
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NP_631906.2:n.39+167693A>T
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NM_001322879.1:c.39+167693A>T
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NP_001309808.1:n.39+167693A>T
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NM_001322880.1:c.39+167693A>T
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NP_001309809.1:n.39+167693A>T
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NM_001322881.1:c.-90+167693A>T
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NP_001309810.1:n.-90+167693A>T
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NM_139167.3:c.39+167693A>T
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NP_631906.2:n.39+167693A>T
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NM_139167.4:c.39+167693A>T
MANE Select
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NP_631906.2:n.39+167693A>T
|
|
NM_001322879.2:c.39+167693A>T
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NP_001309808.1:n.39+167693A>T
|
|
NM_001322880.2:c.39+167693A>T
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NP_001309809.1:n.39+167693A>T
|
|
NM_001322881.2:c.-90+167693A>T
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NP_001309810.1:n.-90+167693A>T
|
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