ENST00000463045.3:c.-79A>G
|
ENSP00000481376.2:n.-79A>G
|
|
ENST00000491274.6:c.51A>G
|
ENSP00000480482.2:p.Thr17=
|
|
ENST00000375499.8:c.93A>G
MANE Select
|
ENSP00000364649.3:p.Thr31=
|
|
ENST00000375499.7:c.93A>G
|
ENSP00000364649.3:p.Thr31=
|
|
ENST00000463045.2:c.-79A>G
|
ENSP00000481376.1:n.-79A>G
|
|
ENST00000466613.2:n.105A>G
|
|
|
ENST00000475506.1:n.10A>G
|
|
|
ENST00000485515.5:n.81A>G
|
|
|
ENST00000491274.5:c.51A>G
|
ENSP00000480482.1:p.Thr17=
|
|
NM_003000.2:c.93A>G , LRG_316t1:c.93A>G
|
NP_002991.2:p.Thr31=
|
|
NM_003000.3:c.93A>G
MANE Select
|
NP_002991.2:p.Thr31=
|
|