ENST00000374580.10:c.1398_1399delinsGA
MANE Select
|
ENSP00000363708.4:p.Trp466=
|
|
ENST00000638587.1:c.1329_1330delinsGA
|
ENSP00000491062.1:p.Trp443=
|
|
ENST00000374574.2:c.1398_1399delinsGA
|
ENSP00000363702.2:p.Trp466=
|
|
ENST00000374580.8:c.1398_1399delinsGA
|
ENSP00000363708.4:p.Trp466=
|
|
NM_001204.6:c.1398_1399delinsGA , LRG_712t1:c.1398_1399delinsGA
|
NP_001195.2:p.Trp466=
|
|
XM_011511687.1:c.1398_1399delinsGA
|
XP_011509989.1:p.Trp466=
|
|
XM_011511688.1:c.1398_1399delinsGA
|
XP_011509990.1:p.Trp466=
|
|
NM_001204.7:c.1398_1399delinsGA
MANE Select
|
NP_001195.2:p.Trp466=
|
|