ENST00000367698.4:c.1361T>A
MANE Select
|
ENSP00000356671.3:p.Phe454Tyr
|
|
ENST00000367698.3:c.1361T>A
|
ENSP00000356671.3:p.Phe454Tyr
|
|
ENST00000617423.4:c.746T>A
|
ENSP00000478688.1:p.Phe249Tyr
|
|
NM_000488.3:c.1361T>A , LRG_577t1:c.1361T>A
|
NP_000479.1:p.Phe454Tyr
|
|
XM_005245198.2:c.1217T>A
|
XP_005245255.1:p.Phe406Tyr
|
|
NM_001365052.1:c.1217T>A
|
NP_001351981.1:p.Phe406Tyr
|
|
NM_000488.4:c.1361T>A
MANE Select
|
NP_000479.1:p.Phe454Tyr
|
|
NM_001365052.2:c.1217T>A
|
NP_001351981.1:p.Phe406Tyr
|
|
NM_001386302.1:c.1484T>A
|
NP_001373231.1:p.Phe495Tyr
|
|
NM_001386303.1:c.1442T>A
|
NP_001373232.1:p.Phe481Tyr
|
|
NM_001386304.1:c.1340T>A
|
NP_001373233.1:p.Phe447Tyr
|
|
NM_001386305.1:c.1304T>A
|
NP_001373234.1:p.Phe435Tyr
|
|
NM_001386306.1:c.1145T>A
|
NP_001373235.1:p.Phe382Tyr
|
|