ENST00000703783.1:n.957C>T
|
|
|
ENST00000703785.1:n.1038C>T
|
|
|
ENST00000262464.9:c.4173C>T
MANE Select
|
ENSP00000262464.4:p.Phe1391=
|
|
ENST00000262464.8:c.4173C>T
|
ENSP00000262464.4:p.Phe1391=
|
|
ENST00000507835.5:c.723C>T
|
ENSP00000426839.1:p.Phe241=
|
|
ENST00000508053.5:c.4173C>T
|
ENSP00000424571.1:p.Phe1391=
|
|
ENST00000508989.5:c.4074C>T
|
ENSP00000425596.1:p.Phe1358=
|
|
ENST00000619499.4:c.4170C>T
|
ENSP00000482132.1:p.Phe1390=
|
|
NM_001999.3:c.4173C>T
|
NP_001990.2:p.Phe1391=
|
|
XM_017009228.2:c.4020C>T
|
XP_016864717.1:p.Phe1340=
|
|
NM_001999.4:c.4173C>T
MANE Select
|
NP_001990.2:p.Phe1391=
|
|