ENST00000698500.1:n.4308C>G
(TTC7A)
|
|
|
ENST00000698503.1:n.2481C>G
(TTC7A)
|
|
|
ENST00000319190.11:c.2475C>G
(TTC7A)
MANE Select
|
ENSP00000316699.5:p.Ala825=
|
|
ENST00000651101.1:n.1073C>G
(TTC7A)
|
|
|
ENST00000651415.1:n.1266C>G
(TTC7A)
|
|
|
ENST00000652236.1:n.1176C>G
(TTC7A)
|
|
|
ENST00000652568.1:n.1148C>G
(TTC7A)
|
|
|
ENST00000319190.9:c.2475C>G
(TTC7A)
|
ENSP00000316699.5:p.Ala825=
|
|
ENST00000394850.6:c.2547C>G
(TTC7A)
|
ENSP00000378320.2:p.Ala849=
|
|
ENST00000409245.5:c.2373C>G
(TTC7A)
|
ENSP00000386307.1:p.Ala791=
|
|
ENST00000409825.5:c.2423C>G
(TTC7A)
|
|
|
ENST00000422269.1:c.787-7684G>C
|
|
|
ENST00000441914.5:c.2316C>G
(TTC7A)
|
|
|
ENST00000464527.2:n.399-7684G>C
(STPG4)
|
|
|
ENST00000482548.1:n.402-5265G>C
(STPG4)
|
|
|
ENST00000484061.5:n.1582C>G
(TTC7A)
|
|
|
ENST00000491786.5:n.1879C>G
(TTC7A)
|
|
|
ENST00000496939.1:n.416-26902G>C
(STPG4)
|
|
|
NM_001288951.1:c.2547C>G
(TTC7A)
|
NP_001275880.1:p.Ala849=
|
|
NM_001288953.1:c.2373C>G
(TTC7A)
|
NP_001275882.1:p.Ala791=
|
|
NM_001288955.1:c.1413C>G
(TTC7A)
|
NP_001275884.1:p.Ala471=
|
|
NM_020458.3:c.2475C>G
(TTC7A)
|
NP_065191.2:p.Ala825=
|
|
XM_005264439.2:c.2118C>G
(TTC7A)
|
XP_005264496.1:p.Ala706=
|
|
XM_011532998.1:c.2118C>G
(TTC7A)
|
XP_011531300.1:p.Ala706=
|
|
XM_011533000.1:c.1695C>G
(TTC7A)
|
XP_011531302.1:p.Ala565=
|
|
XM_011533001.1:c.1428C>G
(TTC7A)
|
XP_011531303.1:p.Ala476=
|
|
XM_005264439.4:c.2118C>G
(TTC7A)
|
XP_005264496.1:p.Ala706=
|
|
XM_011532998.3:c.2118C>G
(TTC7A)
|
XP_011531300.1:p.Ala706=
|
|
XM_011533000.3:c.1695C>G
(TTC7A)
|
XP_011531302.1:p.Ala565=
|
|
XM_011533001.3:c.1428C>G
(TTC7A)
|
XP_011531303.1:p.Ala476=
|
|
XM_017004524.1:c.2358C>G
(TTC7A)
|
XP_016860013.1:p.Ala786=
|
|
XM_017004525.1:c.2307C>G
(TTC7A)
|
XP_016860014.1:p.Ala769=
|
|
XM_017004526.1:c.2226C>G
(TTC7A)
|
XP_016860015.1:p.Ala742=
|
|
XM_024453013.1:c.1440C>G
(TTC7A)
|
XP_024308781.1:p.Ala480=
|
|
NM_020458.4:c.2475C>G
(TTC7A)
MANE Select
|
NP_065191.2:p.Ala825=
|
|
NM_001288951.2:c.2547C>G
(TTC7A)
|
NP_001275880.1:p.Ala849=
|
|
NM_001288953.2:c.2373C>G
(TTC7A)
|
NP_001275882.1:p.Ala791=
|
|
NM_001288955.2:c.1413C>G
(TTC7A)
|
NP_001275884.1:p.Ala471=
|
|