ENST00000232607.7:c.551A>T
MANE Select
|
ENSP00000232607.2:p.Glu184Val
|
|
ENST00000232607.6:c.551A>T
|
ENSP00000232607.2:p.Glu184Val
|
|
ENST00000460034.5:c.*295A>T
|
ENSP00000420409.1:n.*295A>T
|
|
ENST00000462091.5:c.*223A>T
|
ENSP00000417893.1:n.*223A>T
|
|
ENST00000467167.5:c.*449A>T
|
ENSP00000419618.1:n.*449A>T
|
|
ENST00000474588.5:c.311-107A>T
|
ENSP00000420348.1:n.311-107A>T
|
|
ENST00000479719.5:c.551A>T
|
ENSP00000420754.1:p.Glu184Val
|
|
ENST00000497791.5:c.*223A>T
|
ENSP00000419121.1:n.*223A>T
|
|
ENST00000498715.1:n.269A>T
|
|
|
NM_000373.3:c.551A>T
|
NP_000364.1:p.Glu184Val
|
|
NR_033434.1:n.503A>T
|
|
|
NR_033437.1:n.756A>T
|
|
|
XR_001740253.2:n.581A>T
|
|
|
NM_000373.4:c.551A>T
MANE Select
|
NP_000364.1:p.Glu184Val
|
|
NR_033434.2:n.417A>T
|
|
|
NR_033437.2:n.670A>T
|
|
|