ENST00000366971.9:c.1026_1029delinsTATC
MANE Select
|
ENSP00000355938.4:p.Gly342=
|
|
ENST00000366971.8:c.1026_1029delinsTATC
|
ENSP00000355938.4:p.Gly342=
|
|
ENST00000419102.1:c.422_425delinsTATC
|
|
|
ENST00000474693.1:n.251_254delinsTATC
|
|
|
NM_014053.3:c.1026_1029delinsTATC
|
NP_054772.1:p.Gly342=
|
|
XM_011509446.1:c.1026_1029delinsTATC
|
XP_011507748.1:p.Gly342=
|
|
XR_247024.1:n.1200_1203delinsTATC
|
|
|
XR_426771.1:n.1327_1330delinsTATC
|
|
|
XM_011509446.3:c.1026_1029delinsTATC
|
XP_011507748.1:p.Gly342=
|
|
XR_247024.3:n.1200_1203delinsTATC
|
|
|
NM_014053.4:c.1026_1029delinsTATC
MANE Select
|
NP_054772.1:p.Gly342=
|
|