ENST00000375448.4:c.955T>G
MANE Select
|
ENSP00000364597.4:p.Phe319Val
|
|
ENST00000468945.1:n.14T>G
|
|
|
NM_012387.2:c.955T>G
|
NP_036519.2:p.Phe319Val
|
|
XM_011541150.1:c.769T>G
|
XP_011539452.1:p.Phe257Val
|
|
XM_011541151.1:c.955T>G
|
XP_011539453.1:p.Phe319Val
|
|
XM_011541152.1:c.418T>G
|
XP_011539454.1:p.Phe140Val
|
|
XM_011541153.1:c.955T>G
|
XP_011539455.1:p.Phe319Val
|
|
XM_011541154.1:c.955T>G
|
XP_011539456.1:p.Phe319Val
|
|
XM_011541155.1:c.955T>G
|
XP_011539457.1:p.Phe319Val
|
|
XM_011541156.1:c.955T>G
|
XP_011539458.1:p.Phe319Val
|
|
XM_011541157.1:c.64T>G
|
XP_011539459.1:p.Phe22Val
|
|
XM_011541154.2:c.955T>G
|
XP_011539456.1:p.Phe319Val
|
|
NM_012387.3:c.955T>G
MANE Select
|
NP_036519.2:p.Phe319Val
|
|