ENST00000272602.7:c.697G>T
MANE Select
|
ENSP00000272602.2:p.Val233Phe
|
|
ENST00000272602.6:c.697G>T
|
ENSP00000272602.2:p.Val233Phe
|
|
ENST00000393504.5:c.697G>T
|
ENSP00000377140.1:p.Val233Phe
|
|
ENST00000409937.1:c.709G>T
|
ENSP00000386761.1:p.Val237Phe
|
|
ENST00000436404.6:c.643G>T
|
ENSP00000410070.2:p.Val215Phe
|
|
NM_001079878.1:c.643G>T
|
NP_001073347.1:p.Val215Phe
|
|
NM_001298.2:c.697G>T
|
NP_001289.1:p.Val233Phe
|
|
XM_006712243.2:c.808G>T
|
XP_006712306.1:p.Val270Phe
|
|
XM_011510554.1:c.862G>T
|
XP_011508856.1:p.Val288Phe
|
|
XM_011510554.2:c.862G>T
|
XP_011508856.1:p.Val288Phe
|
|
NM_001079878.2:c.643G>T
|
NP_001073347.1:p.Val215Phe
|
|
NM_001298.3:c.697G>T
MANE Select
|
NP_001289.1:p.Val233Phe
|
|