ENST00000399391.7:c.410G>A
|
ENSP00000382323.2:p.Arg137His
|
|
ENST00000399397.6:c.374G>A
MANE Select
|
ENSP00000382329.2:p.Arg125His
|
|
ENST00000399391.6:c.410G>A
|
ENSP00000382323.2:p.Arg137His
|
|
ENST00000399397.5:c.374G>A
|
ENSP00000382329.2:p.Arg125His
|
|
ENST00000428619.1:c.191G>A
|
ENSP00000399057.2:p.Arg64His
|
|
ENST00000498332.5:n.280G>A
|
|
|
NM_001277269.1:c.410G>A
|
NP_001264198.1:p.Arg137His
|
|
NM_001292063.1:c.374G>A
|
NP_001278992.1:p.Arg125His
|
|
NM_001277269.2:c.410G>A
|
NP_001264198.1:p.Arg137His
|
|
NM_001292063.2:c.374G>A
MANE Select
|
NP_001278992.1:p.Arg125His
|
|