ENST00000687461.1:n.288+3875C>T
(IFT122)
|
|
|
ENST00000693654.1:n.355+3875C>T
(IFT122)
|
|
|
ENST00000429544.7:c.537G>A
(MBD4)
MANE Select
|
ENSP00000394080.2:p.Arg179=
|
|
ENST00000249910.5:c.537G>A
(MBD4)
|
ENSP00000249910.1:p.Arg179=
|
|
ENST00000393278.6:c.247+701G>A
(MBD4)
|
ENSP00000376959.2:n.247+701G>A
|
|
ENST00000429544.6:c.537G>A
(MBD4)
|
ENSP00000394080.2:p.Arg179=
|
|
ENST00000503197.5:c.537G>A
(MBD4)
|
ENSP00000424873.1:p.Arg179=
|
|
ENST00000505883.1:n.553G>A
(MBD4)
|
|
|
ENST00000507208.1:c.537G>A
(MBD4)
|
ENSP00000422327.1:p.Arg179=
|
|
ENST00000509587.1:n.442+613G>A
(MBD4)
|
|
|
ENST00000509828.1:c.104+2623G>A
(MBD4)
|
ENSP00000422690.1:n.104+2623G>A
|
|
NM_001276270.1:c.537G>A
(MBD4)
|
NP_001263199.1:p.Arg179=
|
|
NM_001276271.1:c.537G>A
(MBD4)
|
NP_001263200.1:p.Arg179=
|
|
NM_001276272.1:c.537G>A
(MBD4)
|
NP_001263201.1:p.Arg179=
|
|
NM_001276273.1:c.247+701G>A
(MBD4)
|
NP_001263202.1:n.247+701G>A
|
|
NM_003925.2:c.537G>A
(MBD4)
|
NP_003916.1:p.Arg179=
|
|
XM_011513267.1:c.537G>A
(MBD4)
|
XP_011511569.1:p.Arg179=
|
|
XM_011513268.1:c.16+613G>A
(MBD4)
|
XP_011511570.1:n.16+613G>A
|
|
XM_024453810.1:c.537G>A
(MBD4)
|
XP_024309578.1:p.Arg179=
|
|
NM_001276270.2:c.537G>A
(MBD4)
MANE Select
|
NP_001263199.1:p.Arg179=
|
|
NM_001276272.2:c.537G>A
(MBD4)
|
NP_001263201.1:p.Arg179=
|
|
NM_003925.3:c.537G>A
(MBD4)
|
NP_003916.1:p.Arg179=
|
|
NM_001276271.2:c.537G>A
(MBD4)
|
NP_001263200.1:p.Arg179=
|
|
NM_001276273.2:c.247+701G>A
(MBD4)
|
NP_001263202.1:n.247+701G>A
|
|