ENST00000367698.4:c.930C>T
MANE Select
|
ENSP00000356671.3:p.Asp310=
|
|
ENST00000367698.3:c.930C>T
|
ENSP00000356671.3:p.Asp310=
|
|
ENST00000487183.1:n.581C>T
|
|
|
ENST00000617423.4:c.559+2089C>T
|
ENSP00000478688.1:n.559+2089C>T
|
|
NM_000488.3:c.930C>T , LRG_577t1:c.930C>T
|
NP_000479.1:p.Asp310=
|
|
XM_005245198.2:c.786C>T
|
XP_005245255.1:p.Asp262=
|
|
NM_001365052.1:c.786C>T
|
NP_001351981.1:p.Asp262=
|
|
NM_000488.4:c.930C>T
MANE Select
|
NP_000479.1:p.Asp310=
|
|
NM_001365052.2:c.786C>T
|
NP_001351981.1:p.Asp262=
|
|
NM_001386302.1:c.1053C>T
|
NP_001373231.1:p.Asp351=
|
|
NM_001386303.1:c.1011C>T
|
NP_001373232.1:p.Asp337=
|
|
NM_001386304.1:c.909C>T
|
NP_001373233.1:p.Asp303=
|
|
NM_001386305.1:c.873C>T
|
NP_001373234.1:p.Asp291=
|
|
NM_001386306.1:c.714C>T
|
NP_001373235.1:p.Asp238=
|
|