ENST00000367698.4:c.1260dup
MANE Select
|
ENSP00000356671.3:p.Val421CysfsTer?
|
|
ENST00000367698.3:c.1260dup
|
ENSP00000356671.3:p.Val421CysfsTer?
|
|
ENST00000617423.4:c.645dup
|
ENSP00000478688.1:p.Val216CysfsTer?
|
|
NM_000488.3:c.1260dup , LRG_577t1:c.1260dup
|
NP_000479.1:p.Val421CysfsTer?
|
|
XM_005245198.2:c.1116dup
|
XP_005245255.1:p.Val373CysfsTer?
|
|
NM_001365052.1:c.1116dup
|
NP_001351981.1:p.Val373CysfsTer?
|
|
NM_000488.4:c.1260dup
MANE Select
|
NP_000479.1:p.Val421CysfsTer?
|
|
NM_001365052.2:c.1116dup
|
NP_001351981.1:p.Val373CysfsTer?
|
|
NM_001386302.1:c.1383dup
|
NP_001373231.1:p.Val462CysfsTer?
|
|
NM_001386303.1:c.1341dup
|
NP_001373232.1:p.Val448CysfsTer?
|
|
NM_001386304.1:c.1239dup
|
NP_001373233.1:p.Val414CysfsTer?
|
|
NM_001386305.1:c.1203dup
|
NP_001373234.1:p.Val402CysfsTer?
|
|
NM_001386306.1:c.1044dup
|
NP_001373235.1:p.Val349CysfsTer?
|
|