ENST00000414306.6:c.*374G>T
|
ENSP00000394586.1:n.*374G>T
|
|
ENST00000697860.1:n.610G>T
|
|
|
ENST00000697861.1:c.442G>T
|
ENSP00000513460.1:p.Gly148Cys
|
|
ENST00000697862.1:c.*84G>T
|
ENSP00000513461.1:n.*84G>T
|
|
ENST00000697863.1:c.586G>T
|
ENSP00000513462.1:p.Gly196Cys
|
|
ENST00000697864.1:n.1787G>T
|
|
|
ENST00000697865.1:c.586G>T
|
ENSP00000513463.1:p.Gly196Cys
|
|
ENST00000697866.1:c.325G>T
|
ENSP00000513464.1:p.Gly109Cys
|
|
ENST00000697867.1:c.621G>T
|
|
|
ENST00000697868.1:c.*407G>T
|
ENSP00000513466.1:n.*407G>T
|
|
ENST00000697897.1:c.643G>T
|
ENSP00000513469.1:p.Gly215Cys
|
|
ENST00000246868.7:c.643G>T
MANE Select
|
ENSP00000246868.2:p.Gly215Cys
|
|
ENST00000246868.6:c.643G>T
|
ENSP00000246868.2:p.Gly215Cys
|
|
ENST00000414306.5:c.*374G>T
|
ENSP00000394586.1:n.*374G>T
|
|
ENST00000617799.1:c.643G>T
|
ENSP00000483040.1:p.Gly215Cys
|
|
NM_016038.2:c.643G>T , LRG_104t1:c.643G>T
|
NP_057122.2:p.Gly215Cys
|
|
NM_016038.3:c.643G>T
|
NP_057122.2:p.Gly215Cys
|
|
NM_016038.4:c.643G>T
MANE Select
|
NP_057122.2:p.Gly215Cys
|
|