ENST00000367698.4:c.1252_1255dup
MANE Select
|
ENSP00000356671.3:p.Ala419AspfsTer?
|
|
ENST00000367698.3:c.1252_1255dup
|
ENSP00000356671.3:p.Ala419AspfsTer?
|
|
ENST00000617423.4:c.637_640dup
|
ENSP00000478688.1:p.Ala214AspfsTer?
|
|
NM_000488.3:c.1252_1255dup , LRG_577t1:c.1252_1255dup
|
NP_000479.1:p.Ala419AspfsTer?
|
|
XM_005245198.2:c.1108_1111dup
|
XP_005245255.1:p.Ala371AspfsTer?
|
|
NM_001365052.1:c.1108_1111dup
|
NP_001351981.1:p.Ala371AspfsTer?
|
|
NM_000488.4:c.1252_1255dup
MANE Select
|
NP_000479.1:p.Ala419AspfsTer?
|
|
NM_001365052.2:c.1108_1111dup
|
NP_001351981.1:p.Ala371AspfsTer?
|
|
NM_001386302.1:c.1375_1378dup
|
NP_001373231.1:p.Ala460AspfsTer?
|
|
NM_001386303.1:c.1333_1336dup
|
NP_001373232.1:p.Ala446AspfsTer?
|
|
NM_001386304.1:c.1231_1234dup
|
NP_001373233.1:p.Ala412AspfsTer?
|
|
NM_001386305.1:c.1195_1198dup
|
NP_001373234.1:p.Ala400AspfsTer?
|
|
NM_001386306.1:c.1036_1039dup
|
NP_001373235.1:p.Ala347AspfsTer?
|
|