ENST00000395503.9:c.2100+96A>G
MANE Select
|
ENSP00000378879.5:n.2100+96A>G
|
|
ENST00000357084.7:c.2100+96A>G
|
ENSP00000349595.3:n.2100+96A>G
|
|
ENST00000395503.8:c.2100+96A>G
|
ENSP00000378879.4:n.2100+96A>G
|
|
ENST00000536376.5:c.1725+96A>G
|
ENSP00000443101.1:n.1725+96A>G
|
|
NM_001286075.1:c.1725+96A>G
|
NP_001273004.1:n.1725+96A>G
|
|
NM_004320.4:c.2100+96A>G
|
NP_004311.1:n.2100+96A>G
|
|
NM_173201.3:c.2100+96A>G
|
NP_775293.1:n.2100+96A>G
|
|
NM_004320.6:c.2100+96A>G
MANE Select
|
NP_004311.1:n.2100+96A>G
|
|
NM_173201.4:c.2100+96A>G
|
NP_775293.1:n.2100+96A>G
|
|
NM_001286075.2:c.1725+96A>G
|
NP_001273004.1:n.1725+96A>G
|
|
NM_173201.5:c.2100+96A>G
|
NP_775293.1:n.2100+96A>G
|
|