ENST00000232607.7:c.385G>C
MANE Select
|
ENSP00000232607.2:p.Gly129Arg
|
|
ENST00000232607.6:c.385G>C
|
ENSP00000232607.2:p.Gly129Arg
|
|
ENST00000460034.5:c.*129G>C
|
ENSP00000420409.1:n.*129G>C
|
|
ENST00000462091.5:c.*57G>C
|
ENSP00000417893.1:n.*57G>C
|
|
ENST00000467167.5:c.*283G>C
|
ENSP00000419618.1:n.*283G>C
|
|
ENST00000474588.5:c.311-273G>C
|
ENSP00000420348.1:n.311-273G>C
|
|
ENST00000479719.5:c.385G>C
|
ENSP00000420754.1:p.Gly129Arg
|
|
ENST00000497791.5:c.*57G>C
|
ENSP00000419121.1:n.*57G>C
|
|
ENST00000498715.1:n.103G>C
|
|
|
NM_000373.3:c.385G>C
|
NP_000364.1:p.Gly129Arg
|
|
NR_033434.1:n.337G>C
|
|
|
NR_033437.1:n.590G>C
|
|
|
XR_001740253.2:n.415G>C
|
|
|
NM_000373.4:c.385G>C
MANE Select
|
NP_000364.1:p.Gly129Arg
|
|
NR_033434.2:n.251G>C
|
|
|
NR_033437.2:n.504G>C
|
|
|