ENST00000376228.10:c.541_542insCG
MANE Select
|
ENSP00000365402.5:p.Arg181ThrfsTer?
|
|
ENST00000376228.9:c.541_542insCG
|
ENSP00000365402.5:p.Arg181ThrfsTer?
|
|
ENST00000376237.8:c.*128_*129insCG
|
ENSP00000365412.4:n.*128_*129insCG
|
|
ENST00000383329.7:c.541_542insCG
|
ENSP00000372819.3:p.Arg181ThrfsTer?
|
|
ENST00000415537.1:c.539_540insCG
|
|
|
ENST00000484378.1:n.810_811insCG
|
|
|
ENST00000487245.5:n.900_901insCG
|
|
|
ENST00000495835.1:n.730_731insCG
|
|
|
NM_002117.5:c.541_542insCG
|
NP_002108.4:p.Arg181ThrfsTer?
|
|
NM_002117.6:c.541_542insCG
MANE Select
|
NP_002108.4:p.Arg181ThrfsTer?
|
|