ENST00000326448.12:c.1414G>C
(IFT80)
MANE Select
|
ENSP00000312778.7:p.Gly472Arg
|
|
ENST00000326448.11:c.1414G>C
(IFT80)
|
ENSP00000312778.7:p.Gly472Arg
|
|
ENST00000483465.5:c.1003G>C
(IFT80)
|
ENSP00000418196.1:p.Gly335Arg
|
|
ENST00000483754.1:c.1927G>C
(TRIM59-IFT80)
|
ENSP00000456272.1:p.Gly643Arg
|
|
ENST00000487943.5:n.2633G>C
(IFT80)
|
|
|
ENST00000496589.5:c.1003G>C
(IFT80)
|
ENSP00000420646.1:p.Gly335Arg
|
|
NM_001190241.1:c.1003G>C
(IFT80)
|
NP_001177170.1:p.Gly335Arg
|
|
NM_001190242.1:c.1003G>C
(IFT80)
|
NP_001177171.1:p.Gly335Arg
|
|
NM_020800.2:c.1414G>C
(IFT80)
|
NP_065851.1:p.Gly472Arg
|
|
XR_924138.1:n.2900-7092C>G
(C3orf80)
|
|
|
NR_148401.1:n.2122G>C
(TRIM59-IFT80)
|
|
|
NR_148402.1:n.3658G>C
(TRIM59-IFT80)
|
|
|
NR_148403.1:n.3925G>C
(TRIM59-IFT80)
|
|
|
NM_020800.3:c.1414G>C
(IFT80)
MANE Select
|
NP_065851.1:p.Gly472Arg
|
|
NM_001190241.2:c.1003G>C
(IFT80)
|
NP_001177170.1:p.Gly335Arg
|
|
NM_001190242.2:c.1003G>C
(IFT80)
|
NP_001177171.1:p.Gly335Arg
|
|