ENST00000262319.11:c.*518A>G
(TELO2)
MANE Select
|
ENSP00000262319.6:n.*518A>G
|
|
ENST00000426508.7:c.*490T>C
(IFT140)
MANE Select
|
ENSP00000406012.2:n.*490T>C
|
|
ENST00000262319.10:c.*518A>G
(TELO2)
|
ENSP00000262319.6:n.*518A>G
|
|
ENST00000361339.9:c.*490T>C
(IFT140)
|
ENSP00000354895.5:n.*490T>C
|
|
ENST00000397417.6:c.*3317T>C
(IFT140)
|
ENSP00000380562.2:n.*3317T>C
|
|
ENST00000426508.6:c.*490T>C
(IFT140)
|
ENSP00000406012.2:n.*490T>C
|
|
ENST00000565298.5:n.4703T>C
(IFT140)
|
|
|
ENST00000568240.1:n.1324A>G
(TELO2)
|
|
|
NM_014714.3:c.*490T>C
(IFT140)
|
NP_055529.2:n.*490T>C
|
|
NM_016111.3:c.*518A>G
(TELO2)
|
NP_057195.2:n.*518A>G
|
|
XM_006720989.2:c.*490T>C
(IFT140)
|
XP_006721052.1:n.*490T>C
|
|
XM_006720990.2:c.*490T>C
(IFT140)
|
XP_006721053.1:n.*490T>C
|
|
XM_006720991.2:c.*490T>C
(IFT140)
|
XP_006721054.1:n.*490T>C
|
|
XM_006720992.2:c.*490T>C
(IFT140)
|
XP_006721055.1:n.*490T>C
|
|
XM_011522766.1:c.*490T>C
(IFT140)
|
XP_011521068.1:n.*490T>C
|
|
XM_011522767.1:c.*490T>C
(IFT140)
|
XP_011521069.1:n.*490T>C
|
|
XM_011522773.1:c.*518A>G
(TELO2)
|
XP_011521075.1:n.*518A>G
|
|
XM_011522774.1:c.*518A>G
(TELO2)
|
XP_011521076.1:n.*518A>G
|
|
XM_011522775.1:c.*518A>G
(TELO2)
|
XP_011521077.1:n.*518A>G
|
|
XM_011522776.1:c.*518A>G
(TELO2)
|
XP_011521078.1:n.*518A>G
|
|
XR_932982.1:n.3331A>G
(TELO2)
|
|
|
NM_001351846.1:c.*518A>G
(TELO2)
|
NP_001338775.1:n.*518A>G
|
|
XM_006720990.3:c.*490T>C
(IFT140)
|
XP_006721053.1:n.*490T>C
|
|
XM_006720991.3:c.*490T>C
(IFT140)
|
XP_006721054.1:n.*490T>C
|
|
XM_006720992.3:c.*490T>C
(IFT140)
|
XP_006721055.1:n.*490T>C
|
|
XM_011522766.3:c.*490T>C
(IFT140)
|
XP_011521068.1:n.*490T>C
|
|
XM_011522767.2:c.*490T>C
(IFT140)
|
XP_011521069.1:n.*490T>C
|
|
XM_011522773.3:c.*518A>G
(TELO2)
|
XP_011521075.1:n.*518A>G
|
|
XM_011522774.2:c.*518A>G
(TELO2)
|
XP_011521076.1:n.*518A>G
|
|
XM_011522775.3:c.*518A>G
(TELO2)
|
XP_011521077.1:n.*518A>G
|
|
XM_011522776.2:c.*518A>G
(TELO2)
|
XP_011521078.1:n.*518A>G
|
|
XM_017023910.1:c.*490T>C
(IFT140)
|
XP_016879399.1:n.*490T>C
|
|
XM_017023911.1:c.*490T>C
(IFT140)
|
XP_016879400.1:n.*490T>C
|
|
XR_001752042.2:n.3564A>G
(TELO2)
|
|
|
XR_001752043.2:n.3079A>G
(TELO2)
|
|
|
XR_001752044.2:n.3016A>G
(TELO2)
|
|
|
XR_932982.3:n.3109A>G
(TELO2)
|
|
|
NM_014714.4:c.*490T>C
(IFT140)
MANE Select
|
NP_055529.2:n.*490T>C
|
|
NM_016111.4:c.*518A>G
(TELO2)
MANE Select
|
NP_057195.2:n.*518A>G
|
|
NM_001351846.2:c.*518A>G
(TELO2)
|
NP_001338775.1:n.*518A>G
|
|