ENST00000367698.4:c.1016G>T
MANE Select
|
ENSP00000356671.3:p.Trp339Leu
|
|
ENST00000367698.3:c.1016G>T
|
ENSP00000356671.3:p.Trp339Leu
|
|
ENST00000617423.4:c.559+2175G>T
|
ENSP00000478688.1:n.559+2175G>T
|
|
NM_000488.3:c.1016G>T , LRG_577t1:c.1016G>T
|
NP_000479.1:p.Trp339Leu
|
|
XM_005245198.2:c.872G>T
|
XP_005245255.1:p.Trp291Leu
|
|
NM_001365052.1:c.872G>T
|
NP_001351981.1:p.Trp291Leu
|
|
NM_000488.4:c.1016G>T
MANE Select
|
NP_000479.1:p.Trp339Leu
|
|
NM_001365052.2:c.872G>T
|
NP_001351981.1:p.Trp291Leu
|
|
NM_001386302.1:c.1139G>T
|
NP_001373231.1:p.Trp380Leu
|
|
NM_001386303.1:c.1097G>T
|
NP_001373232.1:p.Trp366Leu
|
|
NM_001386304.1:c.995G>T
|
NP_001373233.1:p.Trp332Leu
|
|
NM_001386305.1:c.959G>T
|
NP_001373234.1:p.Trp320Leu
|
|
NM_001386306.1:c.800G>T
|
NP_001373235.1:p.Trp267Leu
|
|