ENST00000527168.6:n.278-34T>G
|
|
|
ENST00000529110.2:c.263-34T>G
|
ENSP00000435349.2:n.263-34T>G
|
|
ENST00000529957.6:n.237-34T>G
|
|
|
ENST00000683366.1:c.179-163T>G
|
ENSP00000507283.1:n.179-163T>G
|
|
ENST00000683887.1:c.193T>G
|
ENSP00000506886.1:p.Trp65Gly
|
|
ENST00000684100.1:n.65T>G
|
|
|
ENST00000684126.1:n.237-34T>G
|
|
|
ENST00000684688.1:n.770T>G
|
|
|
ENST00000204679.9:c.179-34T>G
MANE Select
|
ENSP00000204679.4:n.179-34T>G
|
|
ENST00000204679.8:c.179-34T>G
|
ENSP00000204679.4:n.179-34T>G
|
|
ENST00000526820.5:c.*81-34T>G
|
ENSP00000434413.1:n.*81-34T>G
|
|
ENST00000527076.1:n.1087T>G
|
|
|
ENST00000527168.5:n.270-163T>G
|
|
|
ENST00000529110.1:c.246-34T>G
|
|
|
ENST00000529957.5:n.278-34T>G
|
|
|
NM_032520.4:c.179-34T>G
|
NP_115909.1:n.179-34T>G
|
|
XM_017023782.1:c.193T>G
|
XP_016879271.1:p.Trp65Gly
|
|
XM_017023783.1:c.-182-34T>G
|
XP_016879272.1:n.-182-34T>G
|
|
NM_032520.5:c.179-34T>G
MANE Select
|
NP_115909.1:n.179-34T>G
|
|