|
ENST00000367698.4:c.1075G>T
MANE Select
|
ENSP00000356671.3:p.Asp359Tyr
|
|
|
ENST00000367698.3:c.1075G>T
|
ENSP00000356671.3:p.Asp359Tyr
|
|
|
ENST00000617423.4:c.560-2137G>T
|
ENSP00000478688.1:n.560-2137G>T
|
|
|
NM_000488.3:c.1075G>T , LRG_577t1:c.1075G>T
|
NP_000479.1:p.Asp359Tyr
|
|
|
XM_005245198.2:c.931G>T
|
XP_005245255.1:p.Asp311Tyr
|
|
|
NM_001365052.1:c.931G>T
|
NP_001351981.1:p.Asp311Tyr
|
|
|
NM_000488.4:c.1075G>T
MANE Select
|
NP_000479.1:p.Asp359Tyr
|
|
|
NM_001365052.2:c.931G>T
|
NP_001351981.1:p.Asp311Tyr
|
|
|
NM_001386302.1:c.1198G>T
|
NP_001373231.1:p.Asp400Tyr
|
|
|
NM_001386303.1:c.1156G>T
|
NP_001373232.1:p.Asp386Tyr
|
|
|
NM_001386304.1:c.1054G>T
|
NP_001373233.1:p.Asp352Tyr
|
|
|
NM_001386305.1:c.1018G>T
|
NP_001373234.1:p.Asp340Tyr
|
|
|
NM_001386306.1:c.859G>T
|
NP_001373235.1:p.Asp287Tyr
|
|
