ENST00000477151.2:n.96G=
|
|
|
ENST00000643794.1:c.109G=
|
ENSP00000495765.1:p.Glu37=
|
|
ENST00000651669.1:c.7-99G=
MANE Select
|
ENSP00000499044.1:n.7-99G=
|
|
ENST00000368567.4:c.7-99G=
|
ENSP00000357555.4:n.7-99G=
|
|
ENST00000392558.4:c.7-99G=
|
ENSP00000376341.4:n.7-99G=
|
|
ENST00000477151.1:n.143G=
|
|
|
ENST00000493224.5:n.254G=
|
|
|
NM_001030.4:c.7-99G=
|
NP_001021.1:n.7-99G=
|
|
NM_001030.6:c.7-99G=
MANE Select
|
NP_001021.1:n.7-99G=
|
|
NM_001349946.1:c.-109G=
|
NP_001336875.1:n.-109G=
|
|
NM_001349947.1:c.-109G=
|
NP_001336876.1:n.-109G=
|
|
NM_001349946.2:c.-109G=
|
NP_001336875.1:n.-109G=
|
|
NM_001349947.2:c.-109G=
|
NP_001336876.1:n.-109G=
|
|