ENST00000367698.4:c.1357dup
MANE Select
|
ENSP00000356671.3:p.Ile453AsnfsTer12
|
|
ENST00000367698.3:c.1357dup
|
ENSP00000356671.3:p.Ile453AsnfsTer12
|
|
ENST00000617423.4:c.742dup
|
ENSP00000478688.1:p.Ile248AsnfsTer12
|
|
NM_000488.3:c.1357dup , LRG_577t1:c.1357dup
|
NP_000479.1:p.Ile453AsnfsTer12
|
|
XM_005245198.2:c.1213dup
|
XP_005245255.1:p.Ile405AsnfsTer12
|
|
NM_001365052.1:c.1213dup
|
NP_001351981.1:p.Ile405AsnfsTer12
|
|
NM_000488.4:c.1357dup
MANE Select
|
NP_000479.1:p.Ile453AsnfsTer12
|
|
NM_001365052.2:c.1213dup
|
NP_001351981.1:p.Ile405AsnfsTer12
|
|
NM_001386302.1:c.1480dup
|
NP_001373231.1:p.Ile494AsnfsTer12
|
|
NM_001386303.1:c.1438dup
|
NP_001373232.1:p.Ile480AsnfsTer12
|
|
NM_001386304.1:c.1336dup
|
NP_001373233.1:p.Ile446AsnfsTer12
|
|
NM_001386305.1:c.1300dup
|
NP_001373234.1:p.Ile434AsnfsTer12
|
|
NM_001386306.1:c.1141dup
|
NP_001373235.1:p.Ile381AsnfsTer12
|
|