ENST00000703162.1:n.241A=
|
|
|
ENST00000281043.4:c.892A=
MANE Select
|
ENSP00000281043.3:p.Thr298=
|
|
ENST00000638417.1:c.259A=
|
ENSP00000491476.1:p.Thr87=
|
|
ENST00000281043.3:c.892A=
|
ENSP00000281043.3:p.Thr298=
|
|
NM_001293228.1:c.892A=
|
NP_001280157.1:p.Thr298=
|
|
NM_001293231.1:c.259A=
|
NP_001280160.1:p.Thr87=
|
|
NM_001293233.1:c.*827A=
|
NP_001280162.1:n.*827A=
|
|
NM_005378.5:c.892A=
|
NP_005369.2:p.Thr298=
|
|
NM_005378.6:c.892A=
MANE Select
|
NP_005369.2:p.Thr298=
|
|
NM_001293228.2:c.892A=
|
NP_001280157.1:p.Thr298=
|
|
NM_001293231.2:c.259A=
|
NP_001280160.1:p.Thr87=
|
|
NM_001293233.2:c.*827A=
|
NP_001280162.1:n.*827A=
|
|