ENST00000367698.4:c.855C>T
MANE Select
|
ENSP00000356671.3:p.Tyr285=
|
|
ENST00000367698.3:c.855C>T
|
ENSP00000356671.3:p.Tyr285=
|
|
ENST00000487183.1:n.506C>T
|
|
|
ENST00000617423.4:c.559+2014C>T
|
ENSP00000478688.1:n.559+2014C>T
|
|
NM_000488.3:c.855C>T , LRG_577t1:c.855C>T
|
NP_000479.1:p.Tyr285=
|
|
XM_005245198.2:c.711C>T
|
XP_005245255.1:p.Tyr237=
|
|
NM_001365052.1:c.711C>T
|
NP_001351981.1:p.Tyr237=
|
|
NM_000488.4:c.855C>T
MANE Select
|
NP_000479.1:p.Tyr285=
|
|
NM_001365052.2:c.711C>T
|
NP_001351981.1:p.Tyr237=
|
|
NM_001386302.1:c.978C>T
|
NP_001373231.1:p.Tyr326=
|
|
NM_001386303.1:c.936C>T
|
NP_001373232.1:p.Tyr312=
|
|
NM_001386304.1:c.834C>T
|
NP_001373233.1:p.Tyr278=
|
|
NM_001386305.1:c.798C>T
|
NP_001373234.1:p.Tyr266=
|
|
NM_001386306.1:c.639C>T
|
NP_001373235.1:p.Tyr213=
|
|