ENST00000477151.2:n.292T>C
|
|
|
ENST00000643794.1:c.225T>C
|
ENSP00000495765.1:p.Cys75=
|
|
ENST00000651669.1:c.104T>C
MANE Select
|
ENSP00000499044.1:p.Val35Ala
|
|
ENST00000368567.4:c.104T>C
|
ENSP00000357555.4:p.Val35Ala
|
|
ENST00000392558.4:c.104T>C
|
ENSP00000376341.4:p.Val35Ala
|
|
ENST00000477151.1:n.259T>C
|
|
|
ENST00000493224.5:n.370T>C
|
|
|
NM_001030.4:c.104T>C
|
NP_001021.1:p.Val35Ala
|
|
NM_001030.6:c.104T>C
MANE Select
|
NP_001021.1:p.Val35Ala
|
|
NM_001349946.1:c.8T>C
|
NP_001336875.1:p.Val3Ala
|
|
NM_001349947.1:c.8T>C
|
NP_001336876.1:p.Val3Ala
|
|
NM_001349946.2:c.8T>C
|
NP_001336875.1:p.Val3Ala
|
|
NM_001349947.2:c.8T>C
|
NP_001336876.1:p.Val3Ala
|
|