ENST00000330889.8:c.890T>C
MANE Select
|
ENSP00000329468.3:p.Phe297Ser
|
|
ENST00000330889.7:c.890T>C
|
ENSP00000329468.3:p.Phe297Ser
|
|
ENST00000470962.1:n.310T>C
|
|
|
ENST00000480980.1:n.324T>C
|
|
|
ENST00000580525.5:c.908T>C
|
ENSP00000464121.1:p.Phe303Ser
|
|
ENST00000581285.5:c.806T>C
|
ENSP00000464155.1:p.Phe269Ser
|
|
ENST00000584828.5:c.259T>C
|
|
|
ENST00000584989.1:c.182T>C
|
ENSP00000462634.1:p.Phe61Ser
|
|
ENST00000585130.5:c.*489T>C
|
ENSP00000464120.1:n.*489T>C
|
|
NM_018404.2:c.890T>C
|
NP_060874.1:p.Phe297Ser
|
|
XM_005258008.2:c.908T>C
|
XP_005258065.1:p.Phe303Ser
|
|
XM_005258011.2:c.845T>C
|
XP_005258068.1:p.Phe282Ser
|
|
XM_006721973.2:c.908T>C
|
XP_006722036.1:p.Phe303Ser
|
|
XM_011524993.1:c.905T>C
|
XP_011523295.1:p.Phe302Ser
|
|
XM_011524994.1:c.887T>C
|
XP_011523296.1:p.Phe296Ser
|
|
NM_001346712.1:c.908T>C
|
NP_001333641.1:p.Phe303Ser
|
|
NM_001346714.1:c.887T>C
|
NP_001333643.1:p.Phe296Ser
|
|
NM_001346716.1:c.890T>C
|
NP_001333645.1:p.Phe297Ser
|
|
NR_144488.1:n.1089T>C
|
|
|
XM_024450831.1:c.890T>C
|
XP_024306599.1:p.Phe297Ser
|
|
XM_024450832.1:c.905T>C
|
XP_024306600.1:p.Phe302Ser
|
|
XM_024450833.1:c.845T>C
|
XP_024306601.1:p.Phe282Ser
|
|
XM_024450834.1:c.908T>C
|
XP_024306602.1:p.Phe303Ser
|
|
XM_024450835.1:c.524T>C
|
XP_024306603.1:p.Phe175Ser
|
|
NM_018404.3:c.890T>C
MANE Select
|
NP_060874.1:p.Phe297Ser
|
|
NM_001346712.2:c.908T>C
|
NP_001333641.1:p.Phe303Ser
|
|
NM_001346714.2:c.887T>C
|
NP_001333643.1:p.Phe296Ser
|
|
NM_001346716.2:c.890T>C
|
NP_001333645.1:p.Phe297Ser
|
|
NR_144488.2:n.880T>C
|
|
|