ENST00000519560.6:c.1459+4430C>G
MANE Select
|
ENSP00000430333.2:n.1459+4430C>G
|
|
ENST00000332966.8:c.1459+4430C>G
|
ENSP00000332164.8:n.1459+4430C>G
|
|
ENST00000404867.7:c.1048+4430C>G
|
ENSP00000384890.4:n.1048+4430C>G
|
|
ENST00000519486.5:n.3162+4430C>G
|
|
|
ENST00000519560.5:c.1459+4430C>G
|
ENSP00000430333.1:n.1459+4430C>G
|
|
NM_001271946.1:c.1459+4430C>G
|
NP_001258875.1:n.1459+4430C>G
|
|
NM_003062.3:c.1459+4430C>G
|
NP_003053.1:n.1459+4430C>G
|
|
XM_017009779.1:c.1270+4430C>G
|
XP_016865268.1:n.1270+4430C>G
|
|
NM_001271946.2:c.1459+4430C>G
|
NP_001258875.2:n.1459+4430C>G
|
|
NM_003062.4:c.1459+4430C>G
MANE Select
|
NP_003053.2:n.1459+4430C>G
|
|