ENST00000698500.1:n.4589T=
(TTC7A)
|
|
|
ENST00000698503.1:n.2762T=
(TTC7A)
|
|
|
ENST00000319190.11:c.*179T=
(TTC7A)
MANE Select
|
ENSP00000316699.5:n.*179T=
|
|
ENST00000651101.1:n.1354T=
(TTC7A)
|
|
|
ENST00000651415.1:n.1547T=
(TTC7A)
|
|
|
ENST00000652236.1:n.1457T=
(TTC7A)
|
|
|
ENST00000652568.1:n.1429T=
(TTC7A)
|
|
|
ENST00000319190.9:c.*179T=
(TTC7A)
|
ENSP00000316699.5:n.*179T=
|
|
ENST00000394850.6:c.*179T=
(TTC7A)
|
ENSP00000378320.2:n.*179T=
|
|
ENST00000409825.5:c.2704T=
(TTC7A)
|
|
|
ENST00000422269.1:c.787-7965A=
|
|
|
ENST00000464527.2:n.399-7965A=
(STPG4)
|
|
|
ENST00000482548.1:n.402-5546A=
(STPG4)
|
|
|
ENST00000484061.5:n.1863T=
(TTC7A)
|
|
|
ENST00000491786.5:n.2160T=
(TTC7A)
|
|
|
ENST00000496939.1:n.416-27183A=
(STPG4)
|
|
|
NM_001288951.1:c.*179T=
(TTC7A)
|
NP_001275880.1:n.*179T=
|
|
NM_001288953.1:c.*179T=
(TTC7A)
|
NP_001275882.1:n.*179T=
|
|
NM_001288955.1:c.*179T=
(TTC7A)
|
NP_001275884.1:n.*179T=
|
|
NM_020458.3:c.*179T=
(TTC7A)
|
NP_065191.2:n.*179T=
|
|
XM_005264439.2:c.*179T=
(TTC7A)
|
XP_005264496.1:n.*179T=
|
|
XM_011532998.1:c.*179T=
(TTC7A)
|
XP_011531300.1:n.*179T=
|
|
XM_011533000.1:c.*179T=
(TTC7A)
|
XP_011531302.1:n.*179T=
|
|
XM_011533001.1:c.*179T=
(TTC7A)
|
XP_011531303.1:n.*179T=
|
|
XM_005264439.4:c.*179T=
(TTC7A)
|
XP_005264496.1:n.*179T=
|
|
XM_011532998.3:c.*179T=
(TTC7A)
|
XP_011531300.1:n.*179T=
|
|
XM_011533000.3:c.*179T=
(TTC7A)
|
XP_011531302.1:n.*179T=
|
|
XM_011533001.3:c.*179T=
(TTC7A)
|
XP_011531303.1:n.*179T=
|
|
XM_017004524.1:c.*179T=
(TTC7A)
|
XP_016860013.1:n.*179T=
|
|
XM_017004525.1:c.*179T=
(TTC7A)
|
XP_016860014.1:n.*179T=
|
|
XM_017004526.1:c.*179T=
(TTC7A)
|
XP_016860015.1:n.*179T=
|
|
XM_024453013.1:c.*179T=
(TTC7A)
|
XP_024308781.1:n.*179T=
|
|
NM_020458.4:c.*179T=
(TTC7A)
MANE Select
|
NP_065191.2:n.*179T=
|
|
NM_001288951.2:c.*179T=
(TTC7A)
|
NP_001275880.1:n.*179T=
|
|
NM_001288953.2:c.*179T=
(TTC7A)
|
NP_001275882.1:n.*179T=
|
|
NM_001288955.2:c.*179T=
(TTC7A)
|
NP_001275884.1:n.*179T=
|
|