ENST00000253408.11:c.758C>T
|
ENSP00000253408.5:p.Ala253Val
|
|
ENST00000435360.8:c.758C>T
|
ENSP00000403962.1:p.Ala253Val
|
|
ENST00000253408.10:c.758C>T
|
ENSP00000253408.5:p.Ala253Val
|
|
ENST00000435360.7:c.758C>T
|
ENSP00000403962.1:p.Ala253Val
|
|
ENST00000586127.6:n.1287C>T
|
|
|
ENST00000586793.6:c.758C>T
|
ENSP00000468500.2:p.Ala253Val
|
|
ENST00000587997.6:n.234C>T
|
|
|
ENST00000588735.3:c.758C>T
MANE Select
|
ENSP00000466598.2:p.Ala253Val
|
|
ENST00000591327.2:n.1912C>T
|
|
|
ENST00000592320.6:c.618+437C>T
|
ENSP00000465320.1:n.618+437C>T
|
|
ENST00000638281.1:c.758C>T
|
ENSP00000491088.1:p.Ala253Val
|
|
ENST00000638618.1:c.413C>T
|
ENSP00000492832.1:p.Ala138Val
|
|
ENST00000639277.1:c.758C>T
|
ENSP00000492432.1:p.Ala253Val
|
|
ENST00000640552.1:n.772C>T
|
|
|
ENST00000253408.9:c.758C>T
|
ENSP00000253408.4:p.Ala253Val
|
|
ENST00000376990.8:c.*157C>T
|
ENSP00000366189.4:n.*157C>T
|
|
ENST00000435360.6:c.758C>T
|
ENSP00000403962.1:p.Ala253Val
|
|
ENST00000586793.5:c.758C>T
|
ENSP00000468500.1:p.Ala253Val
|
|
ENST00000587997.5:c.234C>T
|
|
|
ENST00000588316.1:c.662C>T
|
ENSP00000465629.1:p.Ala221Val
|
|
ENST00000588735.1:c.82+2114C>T
|
ENSP00000466598.1:n.82+2114C>T
|
|
ENST00000588957.5:c.26C>T
|
ENSP00000465565.1:p.Ala9Val
|
|
ENST00000590922.1:n.408C>T
|
|
|
ENST00000592320.5:c.618+437C>T
|
ENSP00000465320.1:n.618+437C>T
|
|
NM_001131019.2:c.758C>T
|
NP_001124491.1:p.Ala253Val
|
|
NM_001242376.1:c.758C>T
|
NP_001229305.1:p.Ala253Val
|
|
NM_002055.4:c.758C>T
|
NP_002046.1:p.Ala253Val
|
|
NM_001363846.1:c.758C>T
|
NP_001350775.1:p.Ala253Val
|
|
XM_024450690.1:c.962C>T
|
XP_024306458.1:p.Ala321Val
|
|
XM_024450691.1:c.962C>T
|
XP_024306459.1:p.Ala321Val
|
|
XM_024450692.1:c.962C>T
|
XP_024306460.1:p.Ala321Val
|
|
XM_024450693.1:c.962C>T
|
XP_024306461.1:p.Ala321Val
|
|
NM_002055.5:c.758C>T
MANE Select
|
NP_002046.1:p.Ala253Val
|
|
NM_001131019.3:c.758C>T
|
NP_001124491.1:p.Ala253Val
|
|
NM_001242376.2:c.758C>T
|
NP_001229305.1:p.Ala253Val
|
|
NM_001242376.3:c.758C>T
|
NP_001229305.1:p.Ala253Val
|
|
NM_001363846.2:c.758C>T
|
NP_001350775.1:p.Ala253Val
|
|