ENST00000299314.12:c.483T>C
MANE Select
|
ENSP00000299314.7:p.Phe161=
|
|
ENST00000299314.11:c.483T>C
|
ENSP00000299314.7:p.Phe161=
|
|
ENST00000549940.5:c.483T>C
|
ENSP00000449150.1:p.Phe161=
|
|
ENST00000550352.1:n.277T>C
|
|
|
ENST00000552681.1:c.117T>C
|
ENSP00000449217.1:p.Phe39=
|
|
NM_024312.4:c.483T>C
|
NP_077288.2:p.Phe161=
|
|
XM_006719593.2:c.483T>C
|
XP_006719656.1:p.Phe161=
|
|
XM_011538731.1:c.402T>C
|
XP_011537033.1:p.Phe134=
|
|
XM_006719593.3:c.483T>C
|
XP_006719656.1:p.Phe161=
|
|
XM_011538731.2:c.402T>C
|
XP_011537033.1:p.Phe134=
|
|
XM_017019961.1:c.267T>C
|
XP_016875450.1:p.Phe89=
|
|
XM_017019962.2:c.-868T>C
|
XP_016875451.1:n.-868T>C
|
|
NM_024312.5:c.483T>C
MANE Select
|
NP_077288.2:p.Phe161=
|
|