ENST00000338639.10:c.412dup
MANE Select
|
ENSP00000340278.5:p.His138ProfsTer6
|
|
ENST00000338639.9:c.412dup
|
ENSP00000340278.5:p.His138ProfsTer6
|
|
ENST00000377488.5:c.412dup
|
ENSP00000366708.1:p.His138ProfsTer6
|
|
ENST00000377491.5:c.412dup
|
ENSP00000366711.1:p.His138ProfsTer6
|
|
ENST00000377493.9:c.352dup
|
ENSP00000466242.1:p.His118ProfsTer6
|
|
ENST00000469225.1:c.325dup
|
ENSP00000466756.1:p.His109ProfsTer6
|
|
ENST00000493373.5:c.412dup
|
ENSP00000465404.1:p.His138ProfsTer6
|
|
ENST00000493678.5:c.412dup
|
ENSP00000418770.1:p.His138ProfsTer6
|
|
NM_001123377.1:c.412dup
|
NP_001116849.1:p.His138ProfsTer6
|
|
NM_007262.4:c.412dup
|
NP_009193.2:p.His138ProfsTer6
|
|
XM_005263424.2:c.412dup
|
XP_005263481.1:p.His138ProfsTer6
|
|
XM_005263424.3:c.412dup
|
XP_005263481.1:p.His138ProfsTer6
|
|
NM_007262.5:c.412dup
MANE Select
|
NP_009193.2:p.His138ProfsTer6
|
|
NM_001123377.2:c.412dup
|
NP_001116849.1:p.His138ProfsTer6
|
|