ENST00000382545.5:c.1235_1236insTG
MANE Select
|
ENSP00000371985.3:p.Tyr413AlafsTer24
|
|
ENST00000543874.3:n.105+2141_105+2142insTG
|
|
|
ENST00000639306.1:c.1073_1074insTG
|
ENSP00000492506.1:p.Tyr359AlafsTer24
|
|
ENST00000639680.1:c.76+347_76+348insTG
|
|
|
ENST00000382545.3:c.1235_1236insTG
|
ENSP00000371985.3:p.Tyr413AlafsTer24
|
|
ENST00000541095.1:n.105+2141_105+2142insTG
|
|
|
ENST00000543874.2:n.96+2141_96+2142insTG
|
|
|
NM_000217.2:c.1235_1236insTG
|
NP_000208.2:p.Tyr413AlafsTer24
|
|
NM_000217.3:c.1235_1236insTG
MANE Select
|
NP_000208.2:p.Tyr413AlafsTer24
|
|