|
NM_015662.3:c.4795C>T
(IFT172)
MANE Select
|
NP_056477.1:p.Arg1599Cys
|
|
ENST00000260570.8:c.4795C>T
(IFT172)
MANE Select
|
ENSP00000260570.3:p.Arg1599Cys
|
|
NM_001168364.1:c.*6-352G>A
(KRTCAP3)
|
NP_001161836.1:n.*6-352G>A
|
|
NM_001168364.2:c.*6-352G>A
(KRTCAP3)
|
NP_001161836.1:n.*6-352G>A
|
|
NM_015662.2:c.4795C>T
(IFT172)
|
NP_056477.1:p.Arg1599Cys
|
|
ENST00000260570.7:c.4795C>T
(IFT172)
|
ENSP00000260570.3:p.Arg1599Cys
|
|
ENST00000420854.1:c.367C>T
(IFT172)
|
ENSP00000398633.1:p.Arg123Cys
|
|
ENST00000452499.1:c.195-352G>A
(KRTCAP3)
|
ENSP00000388115.1:n.195-352G>A
|
|
ENST00000479419.1:n.257C>T
(IFT172)
|
|
|
ENST00000480892.1:n.469C>T
(IFT172)
|
|
|
ENST00000494163.1:n.248C>T
(IFT172)
|
|
|
ENST00000507184.5:n.5076C>T
(IFT172)
|
|
|
ENST00000509128.5:c.1213C>T
(IFT172)
|
|
|
ENST00000543753.5:c.*6-352G>A
(KRTCAP3)
|
ENSP00000442400.1:n.*6-352G>A
|
|
ENST00000674594.1:n.1407C>T
(IFT172)
|
|
|
ENST00000674701.1:c.*4308C>T
(IFT172)
|
ENSP00000502275.1:n.*4308C>T
|
|
ENST00000674824.1:c.*3243C>T
(IFT172)
|
ENSP00000501824.1:n.*3243C>T
|
|
ENST00000674932.1:c.*5241C>T
(IFT172)
|
ENSP00000501967.1:n.*5241C>T
|
|
ENST00000675410.1:c.*2784C>T
(IFT172)
|
ENSP00000502030.1:n.*2784C>T
|
|
ENST00000675690.1:c.4729C>T
(IFT172)
|
ENSP00000502283.1:p.Arg1577Cys
|
|
ENST00000676119.1:c.*4021C>T
(IFT172)
|
ENSP00000501701.1:n.*4021C>T
|
|
XM_005264254.1:c.4729C>T
(IFT172)
|
XP_005264311.1:p.Arg1577Cys
|
|
XM_006711986.2:c.4732C>T
(IFT172)
|
XP_006712049.1:p.Arg1578Cys
|
|
XM_006711986.3:c.4732C>T
(IFT172)
|
XP_006712049.1:p.Arg1578Cys
|
|
XM_006711987.1:c.4795C>T
(IFT172)
|
XP_006712050.1:p.Arg1599Cys
|
|
XM_011532757.1:c.4114C>T
(IFT172)
|
XP_011531059.1:p.Arg1372Cys
|
|
XM_011532757.2:c.4114C>T
(IFT172)
|
XP_011531059.1:p.Arg1372Cys
|
|
XM_011532759.1:c.3235C>T
(IFT172)
|
XP_011531061.1:p.Arg1079Cys
|
|
XM_011532759.2:c.3235C>T
(IFT172)
|
XP_011531061.1:p.Arg1079Cys
|
|
XM_011532760.1:c.2860C>T
(IFT172)
|
XP_011531062.1:p.Arg954Cys
|
|
XM_011532760.2:c.2860C>T
(IFT172)
|
XP_011531062.1:p.Arg954Cys
|
|
XM_017003790.1:c.4666C>T
(IFT172)
|
XP_016859279.1:p.Arg1556Cys
|
|
XM_017003791.1:c.4114C>T
(IFT172)
|
XP_016859280.1:p.Arg1372Cys
|
|
XM_017003793.1:c.2932C>T
(IFT172)
|
XP_016859282.1:p.Arg978Cys
|
|
XM_017003794.1:c.2932C>T
(IFT172)
|
XP_016859283.1:p.Arg978Cys
|
|
XM_017003795.1:c.2728C>T
(IFT172)
|
XP_016859284.1:p.Arg910Cys
|
