ENST00000225964.10:c.4197C>A
MANE Select
|
ENSP00000225964.6:p.Arg1399=
|
|
ENST00000225964.9:c.4197C>A
|
ENSP00000225964.5:p.Arg1399=
|
|
NM_000088.3:c.4197C>A , LRG_1t1:c.4197C>A
|
NP_000079.2:p.Arg1399=
|
|
XM_005257058.3:c.3927C>A
|
XP_005257115.2:p.Arg1309=
|
|
XM_005257059.3:c.3279C>A
|
XP_005257116.2:p.Arg1093=
|
|
XM_011524341.1:c.3999C>A
|
XP_011522643.1:p.Arg1333=
|
|
XM_005257058.4:c.3927C>A
|
XP_005257115.2:p.Arg1309=
|
|
XM_005257059.4:c.3279C>A
|
XP_005257116.2:p.Arg1093=
|
|
NM_000088.4:c.4197C>A
MANE Select
|
NP_000079.2:p.Arg1399=
|
|