ENST00000320650.9:c.*580G>A
MANE Select
|
ENSP00000323505.4:n.*580G>A
|
|
ENST00000296545.11:c.*580G>A
|
ENSP00000296545.7:n.*580G>A
|
|
ENST00000320650.8:c.*580G>A
|
ENSP00000323505.4:n.*580G>A
|
|
ENST00000394159.2:c.988G>A
|
ENSP00000377714.1:n.988G>A
|
|
ENST00000477265.5:c.*580G>A
|
ENSP00000436914.1:n.*580G>A
|
|
NM_000585.4:c.*580G>A
|
NP_000576.1:n.*580G>A
|
|
NM_172175.2:c.*580G>A
|
NP_751915.1:n.*580G>A
|
|
NR_037840.2:n.1919G>A
|
|
|
NM_000585.5:c.*580G>A
MANE Select
|
NP_000576.1:n.*580G>A
|
|
NM_172175.3:c.*580G>A
|
NP_751915.1:n.*580G>A
|
|
NR_037840.3:n.1932G>A
|
|
|