ENST00000297056.11:c.834C>T
MANE Select
|
ENSP00000297056.6:p.Cys278=
|
|
ENST00000297056.10:c.834C>T
|
ENSP00000297056.6:p.Cys278=
|
|
ENST00000425398.6:c.542+2262C>T
|
ENSP00000391171.2:n.542+2262C>T
|
|
ENST00000432248.1:c.420-4461C>T
|
ENSP00000410787.1:n.420-4461C>T
|
|
ENST00000436575.5:c.711C>T
|
ENSP00000404785.1:p.Cys237=
|
|
ENST00000454738.5:c.370+2262C>T
|
ENSP00000411746.1:n.370+2262C>T
|
|
NM_001142936.1:c.542+2262C>T
|
NP_001136408.1:n.542+2262C>T
|
|
NM_139179.3:c.834C>T
|
NP_631918.3:p.Cys278=
|
|
NM_139179.4:c.834C>T
MANE Select
|
NP_631918.3:p.Cys278=
|
|
NM_001142936.2:c.542+2262C>T
|
NP_001136408.1:n.542+2262C>T
|
|