ENST00000703783.1:n.607A>G
|
|
|
ENST00000703785.1:n.688A>G
|
|
|
ENST00000262464.9:c.3823A>G
MANE Select
|
ENSP00000262464.4:p.Met1275Val
|
|
ENST00000262464.8:c.3823A>G
|
ENSP00000262464.4:p.Met1275Val
|
|
ENST00000507835.5:c.373A>G
|
ENSP00000426839.1:p.Met125Val
|
|
ENST00000508053.5:c.3823A>G
|
ENSP00000424571.1:p.Met1275Val
|
|
ENST00000508989.5:c.3724A>G
|
ENSP00000425596.1:p.Met1242Val
|
|
ENST00000619499.4:c.3820A>G
|
ENSP00000482132.1:p.Met1274Val
|
|
NM_001999.3:c.3823A>G
|
NP_001990.2:p.Met1275Val
|
|
XM_017009228.2:c.3670A>G
|
XP_016864717.1:p.Met1224Val
|
|
NM_001999.4:c.3823A>G
MANE Select
|
NP_001990.2:p.Met1275Val
|
|