ENST00000392666.6:c.-192+1501A>C
MANE Select
|
ENSP00000376434.1:n.-192+1501A>C
|
|
ENST00000324003.3:c.-192+1501A>C
|
ENSP00000316136.3:n.-192+1501A>C
|
|
ENST00000324036.7:c.-192+851A>C
|
ENSP00000316233.3:n.-192+851A>C
|
|
ENST00000392665.6:c.-22+1501A>C
|
ENSP00000376433.2:n.-22+1501A>C
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|
ENST00000392666.5:c.-192+1501A>C
|
ENSP00000376434.1:n.-192+1501A>C
|
|
ENST00000440599.6:c.-22+851A>C
|
ENSP00000406320.2:n.-22+851A>C
|
|
ENST00000531562.1:n.124+1501A>C
|
|
|
NM_153764.2:c.-22+1501A>C
|
NP_722448.1:n.-22+1501A>C
|
|
NM_153765.2:c.30+851A>C
|
NP_722449.3:n.30+851A>C
|
|
NM_153766.2:c.-192+1501A>C
|
NP_722450.1:n.-192+1501A>C
|
|
NM_153767.3:c.-192+851A>C
|
NP_722451.1:n.-192+851A>C
|
|
XR_001748442.1:n.3533-1078T>G
|
|
|
NM_153764.3:c.-22+1501A>C
|
NP_722448.1:n.-22+1501A>C
|
|
NM_153765.3:c.30+851A>C
|
NP_722449.3:n.30+851A>C
|
|
NM_153766.3:c.-192+1501A>C
MANE Select
|
NP_722450.1:n.-192+1501A>C
|
|
NM_153767.4:c.-192+851A>C
|
NP_722451.1:n.-192+851A>C
|
|