ENST00000358807.8:c.2975T>C
MANE Select
|
ENSP00000351664.3:p.Met992Thr
|
|
ENST00000358577.7:c.2717T>C
|
ENSP00000351385.3:p.Met906Thr
|
|
ENST00000358807.7:c.2975T>C
|
ENSP00000351664.3:p.Met992Thr
|
|
ENST00000456101.6:n.3754T>C
|
|
|
ENST00000465904.1:n.4026T>C
|
|
|
ENST00000630715.2:c.3032T>C
|
ENSP00000486901.1:p.Met1011Thr
|
|
NM_001159291.1:c.2717T>C
|
NP_001152763.1:p.Met906Thr
|
|
NM_001286613.1:c.3032T>C
|
NP_001273542.1:p.Met1011Thr
|
|
NM_022765.3:c.2975T>C
|
NP_073602.3:p.Met992Thr
|
|
NM_022765.4:c.2975T>C
MANE Select
|
NP_073602.3:p.Met992Thr
|
|
NM_001159291.2:c.2717T>C
|
NP_001152763.1:p.Met906Thr
|
|
NM_001286613.2:c.3032T>C
|
NP_001273542.1:p.Met1011Thr
|
|