ENST00000367698.4:c.1395A>T
MANE Select
|
ENSP00000356671.3:p.Ter465Tyr
|
|
ENST00000367698.3:c.1395A>T
|
ENSP00000356671.3:p.Ter465Tyr
|
|
ENST00000617423.4:c.780A>T
|
ENSP00000478688.1:p.Ter260Tyr
|
|
NM_000488.3:c.1395A>T , LRG_577t1:c.1395A>T
|
NP_000479.1:p.Ter465Tyr
|
|
XM_005245198.2:c.1251A>T
|
XP_005245255.1:p.Ter417Tyr
|
|
NM_001365052.1:c.1251A>T
|
NP_001351981.1:p.Ter417Tyr
|
|
NM_000488.4:c.1395A>T
MANE Select
|
NP_000479.1:p.Ter465Tyr
|
|
NM_001365052.2:c.1251A>T
|
NP_001351981.1:p.Ter417Tyr
|
|
NM_001386302.1:c.1518A>T
|
NP_001373231.1:p.Ter506Tyr
|
|
NM_001386303.1:c.1476A>T
|
NP_001373232.1:p.Ter492Tyr
|
|
NM_001386304.1:c.1374A>T
|
NP_001373233.1:p.Ter458Tyr
|
|
NM_001386305.1:c.1338A>T
|
NP_001373234.1:p.Ter446Tyr
|
|
NM_001386306.1:c.1179A>T
|
NP_001373235.1:p.Ter393Tyr
|
|