ENST00000396705.10:c.731T>C
MANE Select
|
ENSP00000379933.4:p.Ile244Thr
|
|
ENST00000229270.8:c.842T>C
|
ENSP00000229270.4:p.Ile281Thr
|
|
ENST00000396705.9:c.731T>C
|
ENSP00000379933.4:p.Ile244Thr
|
|
ENST00000474253.1:n.220T>C
|
|
|
ENST00000488464.6:c.485T>C
|
ENSP00000475620.1:p.Ile162Thr
|
|
ENST00000535434.5:c.485T>C
|
ENSP00000443599.1:p.Ile162Thr
|
|
ENST00000613953.4:c.842T>C
|
ENSP00000484435.1:p.Ile281Thr
|
|
NM_000365.5:c.731T>C
|
NP_000356.1:p.Ile244Thr
|
|
NM_001159287.1:c.842T>C
|
NP_001152759.1:p.Ile281Thr
|
|
NM_001258026.1:c.485T>C
|
NP_001244955.1:p.Ile162Thr
|
|
XR_002957378.1:n.1739T>C
|
|
|
NM_000365.6:c.731T>C
MANE Select
|
NP_000356.1:p.Ile244Thr
|
|
NM_001258026.2:c.485T>C
|
NP_001244955.1:p.Ile162Thr
|
|