ENST00000326448.12:c.1466G>A
(IFT80)
MANE Select
|
ENSP00000312778.7:p.Cys489Tyr
|
|
ENST00000326448.11:c.1466G>A
(IFT80)
|
ENSP00000312778.7:p.Cys489Tyr
|
|
ENST00000483465.5:c.1055G>A
(IFT80)
|
ENSP00000418196.1:p.Cys352Tyr
|
|
ENST00000483754.1:c.1979G>A
(TRIM59-IFT80)
|
ENSP00000456272.1:p.Cys660Tyr
|
|
ENST00000487943.5:n.2685G>A
(IFT80)
|
|
|
ENST00000496589.5:c.1055G>A
(IFT80)
|
ENSP00000420646.1:p.Cys352Tyr
|
|
NM_001190241.1:c.1055G>A
(IFT80)
|
NP_001177170.1:p.Cys352Tyr
|
|
NM_001190242.1:c.1055G>A
(IFT80)
|
NP_001177171.1:p.Cys352Tyr
|
|
NM_020800.2:c.1466G>A
(IFT80)
|
NP_065851.1:p.Cys489Tyr
|
|
XR_924138.1:n.2900-7144C>T
(C3orf80)
|
|
|
NR_148401.1:n.2174G>A
(TRIM59-IFT80)
|
|
|
NR_148402.1:n.3710G>A
(TRIM59-IFT80)
|
|
|
NR_148403.1:n.3977G>A
(TRIM59-IFT80)
|
|
|
NM_020800.3:c.1466G>A
(IFT80)
MANE Select
|
NP_065851.1:p.Cys489Tyr
|
|
NM_001190241.2:c.1055G>A
(IFT80)
|
NP_001177170.1:p.Cys352Tyr
|
|
NM_001190242.2:c.1055G>A
(IFT80)
|
NP_001177171.1:p.Cys352Tyr
|
|