|
ENST00000367698.4:c.1047G>A
MANE Select
|
ENSP00000356671.3:p.Val349=
|
|
|
ENST00000367698.3:c.1047G>A
|
ENSP00000356671.3:p.Val349=
|
|
|
ENST00000617423.4:c.560-2165G>A
|
ENSP00000478688.1:n.560-2165G>A
|
|
|
NM_000488.3:c.1047G>A , LRG_577t1:c.1047G>A
|
NP_000479.1:p.Val349=
|
|
|
XM_005245198.2:c.903G>A
|
XP_005245255.1:p.Val301=
|
|
|
NM_001365052.1:c.903G>A
|
NP_001351981.1:p.Val301=
|
|
|
NM_000488.4:c.1047G>A
MANE Select
|
NP_000479.1:p.Val349=
|
|
|
NM_001365052.2:c.903G>A
|
NP_001351981.1:p.Val301=
|
|
|
NM_001386302.1:c.1170G>A
|
NP_001373231.1:p.Val390=
|
|
|
NM_001386303.1:c.1128G>A
|
NP_001373232.1:p.Val376=
|
|
|
NM_001386304.1:c.1026G>A
|
NP_001373233.1:p.Val342=
|
|
|
NM_001386305.1:c.990G>A
|
NP_001373234.1:p.Val330=
|
|
|
NM_001386306.1:c.831G>A
|
NP_001373235.1:p.Val277=
|
|
