|
ENST00000312438.8:c.676T>C
(CLCF1)
MANE Select
|
ENSP00000309338.7:p.Ter226Arg
|
|
|
ENST00000312438.7:c.676T>C
(CLCF1)
|
ENSP00000309338.7:p.Ter226Arg
|
|
|
ENST00000533438.1:c.646T>C
(CLCF1)
|
ENSP00000434122.1:p.Ter216Arg
|
|
|
ENST00000543494.1:c.16+8386T>C
|
ENSP00000480527.1:n.16+8386T>C
|
|
|
ENST00000622583.4:n.392-22397A>G
(RAD9A)
|
|
|
|
NM_001166212.1:c.646T>C
(CLCF1)
|
NP_001159684.1:p.Ter216Arg
|
|
|
NM_013246.2:c.676T>C
(CLCF1)
|
NP_037378.1:p.Ter226Arg
|
|
|
NR_024469.1:n.424-22397A>G
|
|
|
|
NM_013246.3:c.676T>C
(CLCF1)
MANE Select
|
NP_037378.1:p.Ter226Arg
|
|
|
NM_001166212.2:c.646T>C
(CLCF1)
|
NP_001159684.1:p.Ter216Arg
|
|
