ENST00000698500.1:n.4211G>A
(TTC7A)
|
|
|
ENST00000698503.1:n.2384G>A
(TTC7A)
|
|
|
ENST00000698504.1:n.459G>A
(TTC7A)
|
|
|
ENST00000319190.11:c.2378G>A
(TTC7A)
MANE Select
|
ENSP00000316699.5:p.Gly793Asp
|
|
ENST00000651101.1:n.976G>A
(TTC7A)
|
|
|
ENST00000651415.1:n.1169G>A
(TTC7A)
|
|
|
ENST00000652236.1:n.1079G>A
(TTC7A)
|
|
|
ENST00000652568.1:n.1051G>A
(TTC7A)
|
|
|
ENST00000319190.9:c.2378G>A
(TTC7A)
|
ENSP00000316699.5:p.Gly793Asp
|
|
ENST00000394850.6:c.2450G>A
(TTC7A)
|
ENSP00000378320.2:p.Gly817Asp
|
|
ENST00000409245.5:c.2276G>A
(TTC7A)
|
ENSP00000386307.1:p.Gly759Asp
|
|
ENST00000409825.5:c.2326G>A
(TTC7A)
|
|
|
ENST00000422269.1:c.787-7587C>T
|
|
|
ENST00000441914.5:c.2219G>A
(TTC7A)
|
|
|
ENST00000464527.2:n.399-7587C>T
(STPG4)
|
|
|
ENST00000482548.1:n.402-5168C>T
(STPG4)
|
|
|
ENST00000484061.5:n.1485G>A
(TTC7A)
|
|
|
ENST00000491786.5:n.1782G>A
(TTC7A)
|
|
|
ENST00000496939.1:n.416-26805C>T
(STPG4)
|
|
|
NM_001288951.1:c.2450G>A
(TTC7A)
|
NP_001275880.1:p.Gly817Asp
|
|
NM_001288953.1:c.2276G>A
(TTC7A)
|
NP_001275882.1:p.Gly759Asp
|
|
NM_001288955.1:c.1316G>A
(TTC7A)
|
NP_001275884.1:p.Gly439Asp
|
|
NM_020458.3:c.2378G>A
(TTC7A)
|
NP_065191.2:p.Gly793Asp
|
|
XM_005264439.2:c.2021G>A
(TTC7A)
|
XP_005264496.1:p.Gly674Asp
|
|
XM_011532998.1:c.2021G>A
(TTC7A)
|
XP_011531300.1:p.Gly674Asp
|
|
XM_011533000.1:c.1598G>A
(TTC7A)
|
XP_011531302.1:p.Gly533Asp
|
|
XM_011533001.1:c.1331G>A
(TTC7A)
|
XP_011531303.1:p.Gly444Asp
|
|
XM_005264439.4:c.2021G>A
(TTC7A)
|
XP_005264496.1:p.Gly674Asp
|
|
XM_011532998.3:c.2021G>A
(TTC7A)
|
XP_011531300.1:p.Gly674Asp
|
|
XM_011533000.3:c.1598G>A
(TTC7A)
|
XP_011531302.1:p.Gly533Asp
|
|
XM_011533001.3:c.1331G>A
(TTC7A)
|
XP_011531303.1:p.Gly444Asp
|
|
XM_017004524.1:c.2261G>A
(TTC7A)
|
XP_016860013.1:p.Gly754Asp
|
|
XM_017004525.1:c.2210G>A
(TTC7A)
|
XP_016860014.1:p.Gly737Asp
|
|
XM_017004526.1:c.2129G>A
(TTC7A)
|
XP_016860015.1:p.Gly710Asp
|
|
XM_024453013.1:c.1343G>A
(TTC7A)
|
XP_024308781.1:p.Gly448Asp
|
|
NM_020458.4:c.2378G>A
(TTC7A)
MANE Select
|
NP_065191.2:p.Gly793Asp
|
|
NM_001288951.2:c.2450G>A
(TTC7A)
|
NP_001275880.1:p.Gly817Asp
|
|
NM_001288953.2:c.2276G>A
(TTC7A)
|
NP_001275882.1:p.Gly759Asp
|
|
NM_001288955.2:c.1316G>A
(TTC7A)
|
NP_001275884.1:p.Gly439Asp
|
|