ENST00000344595.10:c.-5+1588G>T
MANE Select
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ENSP00000339435.5:n.-5+1588G>T
|
|
ENST00000344595.9:c.-5+1588G>T
|
ENSP00000339435.5:n.-5+1588G>T
|
|
ENST00000572709.5:c.-5+2128G>T
|
ENSP00000458814.1:n.-5+2128G>T
|
|
ENST00000574987.1:c.-280+1588G>T
|
ENSP00000461343.1:n.-280+1588G>T
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|
ENST00000575840.5:c.-219+1588G>T
|
ENSP00000461589.1:n.-219+1588G>T
|
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ENST00000576620.5:c.-5+1588G>T
|
ENSP00000461125.1:n.-5+1588G>T
|
|
ENST00000576848.1:c.-85+1588G>T
|
ENSP00000476682.1:n.-85+1588G>T
|
|
NM_001304803.1:c.-280+1588G>T
|
NP_001291732.1:n.-280+1588G>T
|
|
NM_021947.2:c.-5+1588G>T
|
NP_068766.1:n.-5+1588G>T
|
|
XM_006721565.2:c.-5+2128G>T
|
XP_006721628.1:n.-5+2128G>T
|
|
XM_011523975.1:c.-5+1588G>T
|
XP_011522277.1:n.-5+1588G>T
|
|
XM_006721565.3:c.-5+2128G>T
|
XP_006721628.1:n.-5+2128G>T
|
|
NM_021947.3:c.-5+1588G>T
MANE Select
|
NP_068766.1:n.-5+1588G>T
|
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