ENST00000593677.2:c.1300+251A>G
|
|
|
ENST00000688602.1:c.2697+251A>G
|
|
|
ENST00000689936.1:c.2669+251A>G
|
|
|
ENST00000359596.8:c.14364+251A>G
MANE Select
|
ENSP00000352608.2:n.14364+251A>G
|
|
ENST00000355481.8:c.14349+251A>G
|
ENSP00000347667.3:n.14349+251A>G
|
|
ENST00000359596.7:c.14364+251A>G
|
ENSP00000352608.2:n.14364+251A>G
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|
ENST00000360985.7:c.14346+251A>G
|
ENSP00000354254.4:n.14346+251A>G
|
|
NM_000540.2:c.14364+251A>G , LRG_766t1:c.14364+251A>G
|
NP_000531.2:n.14364+251A>G
|
|
NM_001042723.1:c.14349+251A>G
|
NP_001036188.1:n.14349+251A>G
|
|
XM_006723317.1:c.14346+251A>G
|
XP_006723380.1:n.14346+251A>G
|
|
XM_006723319.1:c.14331+251A>G
|
XP_006723382.1:n.14331+251A>G
|
|
XM_011527204.1:c.14361+251A>G
|
XP_011525506.1:n.14361+251A>G
|
|
XM_011527205.1:c.14277+251A>G
|
XP_011525507.1:n.14277+251A>G
|
|
XM_006723317.2:c.14346+251A>G
|
XP_006723380.1:n.14346+251A>G
|
|
XM_006723319.2:c.14331+251A>G
|
XP_006723382.1:n.14331+251A>G
|
|
XM_011527205.2:c.14277+251A>G
|
XP_011525507.1:n.14277+251A>G
|
|
NM_000540.3:c.14364+251A>G
MANE Select
|
NP_000531.2:n.14364+251A>G
|
|
NM_001042723.2:c.14349+251A>G
|
NP_001036188.1:n.14349+251A>G
|
|