ENST00000263967.4:c.1664+119C>G
MANE Select
|
ENSP00000263967.3:n.1664+119C>G
|
|
ENST00000462255.2:n.126+119C>G
|
|
|
ENST00000643187.1:c.1664+119C>G
|
ENSP00000493507.1:n.1664+119C>G
|
|
ENST00000674534.1:n.1537C>G
|
|
|
ENST00000674622.1:c.167+119C>G
|
ENSP00000502417.1:n.167+119C>G
|
|
ENST00000675467.1:n.4471+119C>G
|
|
|
ENST00000675786.1:c.*231+119C>G
|
ENSP00000502323.1:n.*231+119C>G
|
|
ENST00000263967.3:c.1664+119C>G
|
ENSP00000263967.3:n.1664+119C>G
|
|
NM_006218.2:c.1664+119C>G , LRG_310t1:c.1664+119C>G
|
NP_006209.2:n.1664+119C>G
|
|
XM_006713658.2:c.1664+119C>G
|
XP_006713721.1:n.1664+119C>G
|
|
XM_011512894.1:c.1664+119C>G
|
XP_011511196.1:n.1664+119C>G
|
|
NM_006218.3:c.1664+119C>G
|
NP_006209.2:n.1664+119C>G
|
|
XM_006713658.4:c.1664+119C>G
|
XP_006713721.1:n.1664+119C>G
|
|
XM_011512894.2:c.1664+119C>G
|
XP_011511196.1:n.1664+119C>G
|
|
NM_006218.4:c.1664+119C>G
MANE Select
|
NP_006209.2:n.1664+119C>G
|
|