ENST00000378888.10:c.1682_1683dup
MANE Select
|
ENSP00000368166.5:p.Ser562AlafsTer?
|
|
ENST00000378888.9:c.1682_1683dup
|
ENSP00000368166.5:p.Ser562AlafsTer?
|
|
ENST00000378891.9:c.1607_1608dup
|
ENSP00000368169.5:p.Ser537AlafsTer?
|
|
ENST00000610709.2:c.929_930dup
|
ENSP00000480077.1:p.Ser311AlafsTer?
|
|
ENST00000631679.1:c.713_714dup
|
ENSP00000488181.1:p.Ser239AlafsTer13
|
|
ENST00000632445.1:c.611_612dup
|
ENSP00000488888.1:p.Ser205AlafsTer13
|
|
NM_004421.2:c.1607_1608dup
|
NP_004412.2:p.Ser537AlafsTer?
|
|
XM_005244731.2:c.1682_1683dup
|
XP_005244788.1:p.Ser562AlafsTer?
|
|
XM_005244732.2:c.1682_1683dup
|
XP_005244789.1:p.Ser562AlafsTer13
|
|
XM_005244733.2:c.1607_1608dup
|
XP_005244790.1:p.Ser537AlafsTer13
|
|
NM_001330311.1:c.1682_1683dup
|
NP_001317240.1:p.Ser562AlafsTer?
|
|
XM_005244732.4:c.1682_1683dup
|
XP_005244789.1:p.Ser562AlafsTer13
|
|
XM_005244733.4:c.1607_1608dup
|
XP_005244790.1:p.Ser537AlafsTer13
|
|
NM_001330311.2:c.1682_1683dup
MANE Select
|
NP_001317240.1:p.Ser562AlafsTer?
|
|
NM_004421.3:c.1607_1608dup
|
NP_004412.2:p.Ser537AlafsTer?
|
|