|
NM_206965.2:c.571G>A
(FTCD)
MANE Select
|
NP_996848.1:p.Gly191Ser
|
|
ENST00000397746.8:c.571G>A
(FTCD)
MANE Select
|
ENSP00000380854.3:p.Gly191Ser
|
|
NM_001320412.1:c.571G>A
(FTCD)
|
NP_001307341.1:p.Gly191Ser
|
|
NM_001320412.2:c.571G>A
(FTCD)
|
NP_001307341.1:p.Gly191Ser
|
|
NM_001350598.1:c.89C>T
(FTCD-AS1)
|
NP_001337527.1:p.Pro30Leu
|
|
NM_006657.2:c.571G>A
(FTCD)
|
NP_006648.1:p.Gly191Ser
|
|
NM_006657.3:c.571G>A
(FTCD)
|
NP_006648.1:p.Gly191Ser
|
|
NM_206965.1:c.571G>A
(FTCD)
|
NP_996848.1:p.Gly191Ser
|
|
NR_170989.1:n.10C>T
(FTCD-AS1)
|
|
|
ENST00000291670.9:c.571G>A
(FTCD)
|
ENSP00000291670.5:p.Gly191Ser
|
|
ENST00000397743.1:c.571G>A
(FTCD)
|
ENSP00000380851.1:p.Gly191Ser
|
|
ENST00000397746.7:c.571G>A
(FTCD)
|
ENSP00000380854.3:p.Gly191Ser
|
|
ENST00000397748.5:c.571G>A
(FTCD)
|
ENSP00000380856.1:p.Gly191Ser
|
|
ENST00000498355.6:n.640G>A
(FTCD)
|
|
|
XM_006723961.2:c.691G>A
(FTCD)
|
XP_006724024.2:p.Gly231Ser
|
|
XM_006723961.4:c.691G>A
(FTCD)
|
XP_006724024.2:p.Gly231Ser
|
|
XM_006723962.2:c.691G>A
(FTCD)
|
XP_006724025.2:p.Gly231Ser
|
|
XM_006723962.4:c.691G>A
(FTCD)
|
XP_006724025.2:p.Gly231Ser
|
|
XM_011529434.1:c.691G>A
(FTCD)
|
XP_011527736.1:p.Gly231Ser
|
|
XM_011529434.3:c.691G>A
(FTCD)
|
XP_011527736.1:p.Gly231Ser
|
|
XM_011529435.1:c.691G>A
(FTCD)
|
XP_011527737.1:p.Gly231Ser
|
|
XM_011529435.3:c.691G>A
(FTCD)
|
XP_011527737.1:p.Gly231Ser
|
|
XM_011529436.1:c.691G>A
(FTCD)
|
XP_011527738.1:p.Gly231Ser
|
|
XM_011529436.3:c.691G>A
(FTCD)
|
XP_011527738.1:p.Gly231Ser
|
|
XM_011529437.1:c.691G>A
(FTCD)
|
XP_011527739.1:p.Gly231Ser
|
|
XM_011529437.3:c.691G>A
(FTCD)
|
XP_011527739.1:p.Gly231Ser
|
|
XM_011529438.1:c.691G>A
(FTCD)
|
XP_011527740.1:p.Gly231Ser
|
|
XM_011529439.1:c.178G>A
(FTCD)
|
XP_011527741.1:p.Gly60Ser
|
|
XM_011529439.2:c.178G>A
(FTCD)
|
XP_011527741.1:p.Gly60Ser
|
|
XM_011529440.1:c.691G>A
(FTCD)
|
XP_011527742.1:p.Gly231Ser
|
|
XM_011529440.3:c.691G>A
(FTCD)
|
XP_011527742.1:p.Gly231Ser
|
|
XR_937433.1:n.874G>A
(FTCD)
|
|
|
XR_937433.3:n.908G>A
(FTCD)
|
|
