ENST00000348974.5:c.1941A>T
|
ENSP00000330021.7:p.Val647=
|
|
ENST00000394236.9:c.1941A>T
MANE Select
|
ENSP00000377783.3:p.Val647=
|
|
ENST00000407433.6:c.1896A>T
|
ENSP00000385794.2:p.Val632=
|
|
ENST00000647936.1:c.*44A>T
|
ENSP00000496822.1:n.*44A>T
|
|
ENST00000648381.1:n.2109A>T
|
|
|
ENST00000648853.1:c.1899A>T
|
ENSP00000497262.1:p.Val633=
|
|
ENST00000650591.1:c.2037A>T
|
ENSP00000497376.1:p.Val679=
|
|
ENST00000394236.7:c.1941A>T
|
ENSP00000377783.3:p.Val647=
|
|
ENST00000407433.5:c.1548A>T
|
ENSP00000385794.1:p.Val516=
|
|
NM_000313.3:c.1941A>T , LRG_572t1:c.1941A>T
|
NP_000304.2:p.Val647=
|
|
NM_001314077.1:c.2037A>T , LRG_572t2:c.2037A>T
|
NP_001301006.1:p.Val679=
|
|
NM_000313.4:c.1941A>T
MANE Select
|
NP_000304.2:p.Val647=
|
|
NM_001314077.2:c.2037A>T
|
NP_001301006.1:p.Val679=
|
|