|
NM_020458.4:c.2444C>T
(TTC7A)
MANE Select
|
NP_065191.2:p.Ala815Val
|
|
ENST00000319190.11:c.2444C>T
(TTC7A)
MANE Select
|
ENSP00000316699.5:p.Ala815Val
|
|
NM_001288951.1:c.2516C>T
(TTC7A)
|
NP_001275880.1:p.Ala839Val
|
|
NM_001288951.2:c.2516C>T
(TTC7A)
|
NP_001275880.1:p.Ala839Val
|
|
NM_001288953.1:c.2342C>T
(TTC7A)
|
NP_001275882.1:p.Ala781Val
|
|
NM_001288953.2:c.2342C>T
(TTC7A)
|
NP_001275882.1:p.Ala781Val
|
|
NM_001288955.1:c.1382C>T
(TTC7A)
|
NP_001275884.1:p.Ala461Val
|
|
NM_001288955.2:c.1382C>T
(TTC7A)
|
NP_001275884.1:p.Ala461Val
|
|
NM_020458.3:c.2444C>T
(TTC7A)
|
NP_065191.2:p.Ala815Val
|
|
ENST00000319190.9:c.2444C>T
(TTC7A)
|
ENSP00000316699.5:p.Ala815Val
|
|
ENST00000394850.6:c.2516C>T
(TTC7A)
|
ENSP00000378320.2:p.Ala839Val
|
|
ENST00000409245.5:c.2342C>T
(TTC7A)
|
ENSP00000386307.1:p.Ala781Val
|
|
ENST00000409825.5:c.2392C>T
(TTC7A)
|
|
|
ENST00000422269.1:c.787-7653G>A
|
|
|
ENST00000441914.5:c.2285C>T
(TTC7A)
|
|
|
ENST00000464527.2:n.399-7653G>A
(STPG4)
|
|
|
ENST00000482548.1:n.402-5234G>A
(STPG4)
|
|
|
ENST00000484061.5:n.1551C>T
(TTC7A)
|
|
|
ENST00000491786.5:n.1848C>T
(TTC7A)
|
|
|
ENST00000496939.1:n.416-26871G>A
(STPG4)
|
|
|
ENST00000651101.1:n.1042C>T
(TTC7A)
|
|
|
ENST00000651415.1:n.1235C>T
(TTC7A)
|
|
|
ENST00000652236.1:n.1145C>T
(TTC7A)
|
|
|
ENST00000652568.1:n.1117C>T
(TTC7A)
|
|
|
ENST00000698500.1:n.4277C>T
(TTC7A)
|
|
|
ENST00000698503.1:n.2450C>T
(TTC7A)
|
|
|
ENST00000698504.1:n.525C>T
(TTC7A)
|
|
|
XM_005264439.2:c.2087C>T
(TTC7A)
|
XP_005264496.1:p.Ala696Val
|
|
XM_005264439.4:c.2087C>T
(TTC7A)
|
XP_005264496.1:p.Ala696Val
|
|
XM_011532998.1:c.2087C>T
(TTC7A)
|
XP_011531300.1:p.Ala696Val
|
|
XM_011532998.3:c.2087C>T
(TTC7A)
|
XP_011531300.1:p.Ala696Val
|
|
XM_011533000.1:c.1664C>T
(TTC7A)
|
XP_011531302.1:p.Ala555Val
|
|
XM_011533000.3:c.1664C>T
(TTC7A)
|
XP_011531302.1:p.Ala555Val
|
|
XM_011533001.1:c.1397C>T
(TTC7A)
|
XP_011531303.1:p.Ala466Val
|
|
XM_011533001.3:c.1397C>T
(TTC7A)
|
XP_011531303.1:p.Ala466Val
|
|
XM_017004524.1:c.2327C>T
(TTC7A)
|
XP_016860013.1:p.Ala776Val
|
|
XM_017004525.1:c.2276C>T
(TTC7A)
|
XP_016860014.1:p.Ala759Val
|
|
XM_017004526.1:c.2195C>T
(TTC7A)
|
XP_016860015.1:p.Ala732Val
|
|
XM_024453013.1:c.1409C>T
(TTC7A)
|
XP_024308781.1:p.Ala470Val
|
