ENST00000367698.4:c.1021G>T
MANE Select
|
ENSP00000356671.3:p.Asp341Tyr
|
|
ENST00000367698.3:c.1021G>T
|
ENSP00000356671.3:p.Asp341Tyr
|
|
ENST00000617423.4:c.559+2180G>T
|
ENSP00000478688.1:n.559+2180G>T
|
|
NM_000488.3:c.1021G>T , LRG_577t1:c.1021G>T
|
NP_000479.1:p.Asp341Tyr
|
|
XM_005245198.2:c.877G>T
|
XP_005245255.1:p.Asp293Tyr
|
|
NM_001365052.1:c.877G>T
|
NP_001351981.1:p.Asp293Tyr
|
|
NM_000488.4:c.1021G>T
MANE Select
|
NP_000479.1:p.Asp341Tyr
|
|
NM_001365052.2:c.877G>T
|
NP_001351981.1:p.Asp293Tyr
|
|
NM_001386302.1:c.1144G>T
|
NP_001373231.1:p.Asp382Tyr
|
|
NM_001386303.1:c.1102G>T
|
NP_001373232.1:p.Asp368Tyr
|
|
NM_001386304.1:c.1000G>T
|
NP_001373233.1:p.Asp334Tyr
|
|
NM_001386305.1:c.964G>T
|
NP_001373234.1:p.Asp322Tyr
|
|
NM_001386306.1:c.805G>T
|
NP_001373235.1:p.Asp269Tyr
|
|