ENST00000232607.7:c.327A>C
MANE Select
|
ENSP00000232607.2:p.Val109=
|
|
ENST00000232607.6:c.327A>C
|
ENSP00000232607.2:p.Val109=
|
|
ENST00000460034.5:c.*71A>C
|
ENSP00000420409.1:n.*71A>C
|
|
ENST00000462091.5:c.173A>C
|
ENSP00000417893.1:p.Ter58Ser
|
|
ENST00000467167.5:c.*225A>C
|
ENSP00000419618.1:n.*225A>C
|
|
ENST00000474588.5:c.311-331A>C
|
ENSP00000420348.1:n.311-331A>C
|
|
ENST00000479719.5:c.327A>C
|
ENSP00000420754.1:p.Val109=
|
|
ENST00000497791.5:c.173A>C
|
ENSP00000419121.1:p.Ter58Ser
|
|
ENST00000498715.1:n.45A>C
|
|
|
NM_000373.3:c.327A>C
|
NP_000364.1:p.Val109=
|
|
NR_033434.1:n.279A>C
|
|
|
NR_033437.1:n.532A>C
|
|
|
XR_001740253.2:n.357A>C
|
|
|
NM_000373.4:c.327A>C
MANE Select
|
NP_000364.1:p.Val109=
|
|
NR_033434.2:n.193A>C
|
|
|
NR_033437.2:n.446A>C
|
|
|