ENST00000326448.12:c.1441T>G
(IFT80)
MANE Select
|
ENSP00000312778.7:p.Phe481Val
|
|
ENST00000326448.11:c.1441T>G
(IFT80)
|
ENSP00000312778.7:p.Phe481Val
|
|
ENST00000483465.5:c.1030T>G
(IFT80)
|
ENSP00000418196.1:p.Phe344Val
|
|
ENST00000483754.1:c.1954T>G
(TRIM59-IFT80)
|
ENSP00000456272.1:p.Phe652Val
|
|
ENST00000487943.5:n.2660T>G
(IFT80)
|
|
|
ENST00000496589.5:c.1030T>G
(IFT80)
|
ENSP00000420646.1:p.Phe344Val
|
|
NM_001190241.1:c.1030T>G
(IFT80)
|
NP_001177170.1:p.Phe344Val
|
|
NM_001190242.1:c.1030T>G
(IFT80)
|
NP_001177171.1:p.Phe344Val
|
|
NM_020800.2:c.1441T>G
(IFT80)
|
NP_065851.1:p.Phe481Val
|
|
XR_924138.1:n.2900-7119A>C
(C3orf80)
|
|
|
NR_148401.1:n.2149T>G
(TRIM59-IFT80)
|
|
|
NR_148402.1:n.3685T>G
(TRIM59-IFT80)
|
|
|
NR_148403.1:n.3952T>G
(TRIM59-IFT80)
|
|
|
NM_020800.3:c.1441T>G
(IFT80)
MANE Select
|
NP_065851.1:p.Phe481Val
|
|
NM_001190241.2:c.1030T>G
(IFT80)
|
NP_001177170.1:p.Phe344Val
|
|
NM_001190242.2:c.1030T>G
(IFT80)
|
NP_001177171.1:p.Phe344Val
|
|