ENST00000399391.7:c.492T>C
|
ENSP00000382323.2:p.Asp164=
|
|
ENST00000399397.6:c.456T>C
MANE Select
|
ENSP00000382329.2:p.Asp152=
|
|
ENST00000399391.6:c.492T>C
|
ENSP00000382323.2:p.Asp164=
|
|
ENST00000399397.5:c.456T>C
|
ENSP00000382329.2:p.Asp152=
|
|
ENST00000428619.1:c.273T>C
|
ENSP00000399057.2:p.Asp91=
|
|
ENST00000498332.5:n.362T>C
|
|
|
NM_001277269.1:c.492T>C
|
NP_001264198.1:p.Asp164=
|
|
NM_001292063.1:c.456T>C
|
NP_001278992.1:p.Asp152=
|
|
NM_001277269.2:c.492T>C
|
NP_001264198.1:p.Asp164=
|
|
NM_001292063.2:c.456T>C
MANE Select
|
NP_001278992.1:p.Asp152=
|
|