ENST00000399391.7:c.339C>G
|
ENSP00000382323.2:p.Ser113=
|
|
ENST00000399397.6:c.303C>G
MANE Select
|
ENSP00000382329.2:p.Ser101=
|
|
ENST00000399391.6:c.339C>G
|
ENSP00000382323.2:p.Ser113=
|
|
ENST00000399397.5:c.303C>G
|
ENSP00000382329.2:p.Ser101=
|
|
ENST00000428619.1:c.120C>G
|
ENSP00000399057.2:p.Ser40=
|
|
ENST00000498332.5:n.209C>G
|
|
|
NM_001277269.1:c.339C>G
|
NP_001264198.1:p.Ser113=
|
|
NM_001292063.1:c.303C>G
|
NP_001278992.1:p.Ser101=
|
|
NM_001277269.2:c.339C>G
|
NP_001264198.1:p.Ser113=
|
|
NM_001292063.2:c.303C>G
MANE Select
|
NP_001278992.1:p.Ser101=
|
|