ENST00000477151.2:n.298G>C
|
|
|
ENST00000643794.1:c.231G>C
|
ENSP00000495765.1:p.Met77Ile
|
|
ENST00000651669.1:c.110G>C
MANE Select
|
ENSP00000499044.1:p.Cys37Ser
|
|
ENST00000368567.4:c.110G>C
|
ENSP00000357555.4:p.Cys37Ser
|
|
ENST00000392558.4:c.110G>C
|
ENSP00000376341.4:p.Cys37Ser
|
|
ENST00000477151.1:n.265G>C
|
|
|
ENST00000493224.5:n.376G>C
|
|
|
NM_001030.4:c.110G>C
|
NP_001021.1:p.Cys37Ser
|
|
NM_001030.6:c.110G>C
MANE Select
|
NP_001021.1:p.Cys37Ser
|
|
NM_001349946.1:c.14G>C
|
NP_001336875.1:p.Cys5Ser
|
|
NM_001349947.1:c.14G>C
|
NP_001336876.1:p.Cys5Ser
|
|
NM_001349946.2:c.14G>C
|
NP_001336875.1:p.Cys5Ser
|
|
NM_001349947.2:c.14G>C
|
NP_001336876.1:p.Cys5Ser
|
|