ENST00000298573.9:c.368-3897T>G
MANE Select
|
ENSP00000298573.5:n.368-3897T>G
|
|
ENST00000228862.3:c.367+15283T>G
|
ENSP00000228862.3:n.367+15283T>G
|
|
ENST00000298573.8:c.368-3897T>G
|
ENSP00000298573.5:n.368-3897T>G
|
|
ENST00000545864.1:n.100+1509T>G
|
|
|
NM_030640.2:c.368-3897T>G
|
NP_085143.1:n.368-3897T>G
|
|
XM_005253488.1:c.87+15283T>G
|
XP_005253545.1:n.87+15283T>G
|
|
XM_006719155.2:c.368-3897T>G
|
XP_006719218.1:n.368-3897T>G
|
|
XM_011520856.1:c.368-3897T>G
|
XP_011519158.1:n.368-3897T>G
|
|
XM_011520857.1:c.368-3897T>G
|
XP_011519159.1:n.368-3897T>G
|
|
XM_005253488.3:c.87+15283T>G
|
XP_005253545.1:n.87+15283T>G
|
|
XM_017019988.1:c.87+15283T>G
|
XP_016875477.1:n.87+15283T>G
|
|
NM_030640.3:c.368-3897T>G
MANE Select
|
NP_085143.1:n.368-3897T>G
|
|