ENST00000232607.7:c.376G>T
MANE Select
|
ENSP00000232607.2:p.Val126Phe
|
|
ENST00000232607.6:c.376G>T
|
ENSP00000232607.2:p.Val126Phe
|
|
ENST00000460034.5:c.*120G>T
|
ENSP00000420409.1:n.*120G>T
|
|
ENST00000462091.5:c.*48G>T
|
ENSP00000417893.1:n.*48G>T
|
|
ENST00000467167.5:c.*274G>T
|
ENSP00000419618.1:n.*274G>T
|
|
ENST00000474588.5:c.311-282G>T
|
ENSP00000420348.1:n.311-282G>T
|
|
ENST00000479719.5:c.376G>T
|
ENSP00000420754.1:p.Val126Phe
|
|
ENST00000497791.5:c.*48G>T
|
ENSP00000419121.1:n.*48G>T
|
|
ENST00000498715.1:n.94G>T
|
|
|
NM_000373.3:c.376G>T
|
NP_000364.1:p.Val126Phe
|
|
NR_033434.1:n.328G>T
|
|
|
NR_033437.1:n.581G>T
|
|
|
XR_001740253.2:n.406G>T
|
|
|
NM_000373.4:c.376G>T
MANE Select
|
NP_000364.1:p.Val126Phe
|
|
NR_033434.2:n.242G>T
|
|
|
NR_033437.2:n.495G>T
|
|
|