ENST00000553106.6:c.1177_1178insT
MANE Select
|
ENSP00000448059.1:p.Asn393IlefsTer2
|
|
ENST00000307000.7:c.1162_1163insT
|
ENSP00000303500.2:p.Asn388IlefsTer2
|
|
ENST00000549247.6:n.936_937insT
|
|
|
ENST00000551114.2:n.839_840insT
|
|
|
ENST00000553106.5:c.1177_1178insT
|
ENSP00000448059.1:p.Asn393IlefsTer2
|
|
ENST00000635477.1:c.281_282insT
|
|
|
ENST00000635528.1:n.692_693insT
|
|
|
NM_000277.1:c.1177_1178insT
|
NP_000268.1:p.Asn393IlefsTer2
|
|
XM_011538422.1:c.1120_1121insT
|
XP_011536724.1:p.Asn374IlefsTer2
|
|
NM_000277.2:c.1177_1178insT
|
NP_000268.1:p.Asn393IlefsTer2
|
|
NM_001354304.1:c.1177_1178insT
|
NP_001341233.1:p.Asn393IlefsTer2
|
|
NM_000277.3:c.1177_1178insT
MANE Select
|
NP_000268.1:p.Asn393IlefsTer2
|
|
NM_001354304.2:c.1177_1178insT
|
NP_001341233.1:p.Asn393IlefsTer2
|
|