ENST00000321348.9:c.708T>C
MANE Select
|
ENSP00000319141.4:p.His236=
|
|
ENST00000321348.8:c.708T>C
|
ENSP00000319141.4:p.His236=
|
|
ENST00000375252.3:c.*25T>C
|
ENSP00000364401.3:n.*25T>C
|
|
ENST00000409484.5:c.534T>C
|
ENSP00000386739.1:p.His178=
|
|
NM_001127383.1:c.*25T>C
|
NP_001120855.1:n.*25T>C
|
|
NM_001256909.1:c.534T>C
|
NP_001243838.1:p.His178=
|
|
NM_024843.3:c.708T>C
|
NP_079119.3:p.His236=
|
|
NM_024843.4:c.708T>C
MANE Select
|
NP_079119.3:p.His236=
|
|
NM_001127383.2:c.*25T>C
|
NP_001120855.1:n.*25T>C
|
|
NM_001256909.2:c.534T>C
|
NP_001243838.1:p.His178=
|
|