ENST00000216373.10:c.2161+375_2161+389delinsGGCATGAGCCACCAT
MANE Select
|
ENSP00000216373.5:n.2161+375_2161+389delinsGGCATGAGCCACCAT
|
|
ENST00000216373.9:c.2161+375_2161+389delinsGGCATGAGCCACCAT
|
ENSP00000216373.5:n.2161+375_2161+389delinsGGCATGAGCCACCAT
|
|
ENST00000543680.5:c.2062+375_2062+389delinsGGCATGAGCCACCAT
|
ENSP00000445328.1:n.2062+375_2062+389delinsGGCATGAGCCACCAT
|
|
NM_006939.2:c.2161+375_2161+389delinsGGCATGAGCCACCAT
|
NP_008870.2:n.2161+375_2161+389delinsGGCATGAGCCACCAT
|
|
XM_005268021.1:c.1981+375_1981+389delinsGGCATGAGCCACCAT
|
XP_005268078.1:n.1981+375_1981+389delinsGGCATGAGCCACCAT
|
|
XM_011537103.1:c.2122+375_2122+389delinsGGCATGAGCCACCAT
|
XP_011535405.1:n.2122+375_2122+389delinsGGCATGAGCCACCAT
|
|
XM_011537104.1:c.2161+375_2161+389delinsGGCATGAGCCACCAT
|
XP_011535406.1:n.2161+375_2161+389delinsGGCATGAGCCACCAT
|
|
NM_006939.3:c.2161+375_2161+389delinsGGCATGAGCCACCAT
|
NP_008870.2:n.2161+375_2161+389delinsGGCATGAGCCACCAT
|
|
NM_006939.4:c.2161+375_2161+389delinsGGCATGAGCCACCAT
MANE Select
|
NP_008870.2:n.2161+375_2161+389delinsGGCATGAGCCACCAT
|
|