ENST00000297784.10:c.268G>T
MANE Select
|
ENSP00000297784.6:p.Glu90Ter
|
|
ENST00000644967.1:c.-77+5835G>T
|
ENSP00000496159.1:n.-77+5835G>T
|
|
ENST00000645053.1:c.-77+5835G>T
|
ENSP00000493838.1:n.-77+5835G>T
|
|
ENST00000645208.2:c.268G>T
|
ENSP00000494684.1:p.Glu90Ter
|
|
ENST00000645773.1:c.236+5835G>T
|
ENSP00000493698.1:n.236+5835G>T
|
|
ENST00000645787.1:n.308G>T
|
|
|
ENST00000646244.1:n.718G>T
|
|
|
ENST00000646619.1:c.-77+5835G>T
|
ENSP00000493726.1:n.-77+5835G>T
|
|
ENST00000650689.1:n.660+5835G>T
|
|
|
ENST00000651183.1:c.-77+5835G>T
|
ENSP00000498723.1:n.-77+5835G>T
|
|
ENST00000297784.9:c.268G>T
|
ENSP00000297784.5:p.Glu90Ter
|
|
ENST00000340019.4:c.268G>T
|
ENSP00000341433.3:p.Glu90Ter
|
|
NM_138691.2:c.268G>T
|
NP_619636.2:p.Glu90Ter
|
|
XM_011518213.1:c.856G>T
|
XP_011516515.1:p.Glu286Ter
|
|
XM_017014256.1:c.271G>T
|
XP_016869745.1:p.Glu91Ter
|
|
NM_138691.3:c.268G>T
MANE Select
|
NP_619636.2:p.Glu90Ter
|
|