ENST00000367698.4:c.1247dup
MANE Select
|
ENSP00000356671.3:p.Ser417LysfsTer?
|
|
ENST00000367698.3:c.1247dup
|
ENSP00000356671.3:p.Ser417LysfsTer?
|
|
ENST00000617423.4:c.632dup
|
ENSP00000478688.1:p.Ser212LysfsTer?
|
|
NM_000488.3:c.1247dup , LRG_577t1:c.1247dup
|
NP_000479.1:p.Ser417LysfsTer?
|
|
XM_005245198.2:c.1103dup
|
XP_005245255.1:p.Ser369LysfsTer?
|
|
NM_001365052.1:c.1103dup
|
NP_001351981.1:p.Ser369LysfsTer?
|
|
NM_000488.4:c.1247dup
MANE Select
|
NP_000479.1:p.Ser417LysfsTer?
|
|
NM_001365052.2:c.1103dup
|
NP_001351981.1:p.Ser369LysfsTer?
|
|
NM_001386302.1:c.1370dup
|
NP_001373231.1:p.Ser458LysfsTer?
|
|
NM_001386303.1:c.1328dup
|
NP_001373232.1:p.Ser444LysfsTer?
|
|
NM_001386304.1:c.1226dup
|
NP_001373233.1:p.Ser410LysfsTer?
|
|
NM_001386305.1:c.1190dup
|
NP_001373234.1:p.Ser398LysfsTer?
|
|
NM_001386306.1:c.1031dup
|
NP_001373235.1:p.Ser345LysfsTer?
|
|