ENST00000374580.10:c.2558_2559insA
MANE Select
|
ENSP00000363708.4:p.Glu854Ter
|
|
ENST00000638587.1:c.2489_2490insA
|
ENSP00000491062.1:n.2489_2490insA
|
|
ENST00000374574.2:c.1586+3335_1586+3336insA
|
ENSP00000363702.2:n.1586+3335_1586+3336insA
|
|
ENST00000374580.8:c.2558_2559insA
|
ENSP00000363708.4:p.Glu854Ter
|
|
NM_001204.6:c.2558_2559insA , LRG_712t1:c.2558_2559insA
|
NP_001195.2:p.Glu854Ter
|
|
XM_011511687.1:c.2558_2559insA
|
XP_011509989.1:p.Glu854Ter
|
|
XM_011511688.1:c.1586+3335_1586+3336insA
|
XP_011509990.1:n.1586+3335_1586+3336insA
|
|
NM_001204.7:c.2558_2559insA
MANE Select
|
NP_001195.2:p.Glu854Ter
|
|