ENST00000367698.4:c.869T>A
MANE Select
|
ENSP00000356671.3:p.Phe290Tyr
|
|
ENST00000367698.3:c.869T>A
|
ENSP00000356671.3:p.Phe290Tyr
|
|
ENST00000487183.1:n.520T>A
|
|
|
ENST00000617423.4:c.559+2028T>A
|
ENSP00000478688.1:n.559+2028T>A
|
|
NM_000488.3:c.869T>A , LRG_577t1:c.869T>A
|
NP_000479.1:p.Phe290Tyr
|
|
XM_005245198.2:c.725T>A
|
XP_005245255.1:p.Phe242Tyr
|
|
NM_001365052.1:c.725T>A
|
NP_001351981.1:p.Phe242Tyr
|
|
NM_000488.4:c.869T>A
MANE Select
|
NP_000479.1:p.Phe290Tyr
|
|
NM_001365052.2:c.725T>A
|
NP_001351981.1:p.Phe242Tyr
|
|
NM_001386302.1:c.992T>A
|
NP_001373231.1:p.Phe331Tyr
|
|
NM_001386303.1:c.950T>A
|
NP_001373232.1:p.Phe317Tyr
|
|
NM_001386304.1:c.848T>A
|
NP_001373233.1:p.Phe283Tyr
|
|
NM_001386305.1:c.812T>A
|
NP_001373234.1:p.Phe271Tyr
|
|
NM_001386306.1:c.653T>A
|
NP_001373235.1:p.Phe218Tyr
|
|