ENST00000348974.5:c.1989T>C
|
ENSP00000330021.7:p.Ala663=
|
|
ENST00000394236.9:c.1989T>C
MANE Select
|
ENSP00000377783.3:p.Ala663=
|
|
ENST00000407433.6:c.1944T>C
|
ENSP00000385794.2:p.Ala648=
|
|
ENST00000647936.1:c.*92T>C
|
ENSP00000496822.1:n.*92T>C
|
|
ENST00000648381.1:n.2157T>C
|
|
|
ENST00000648853.1:c.1947T>C
|
ENSP00000497262.1:p.Ala649=
|
|
ENST00000650591.1:c.2085T>C
|
ENSP00000497376.1:p.Ala695=
|
|
ENST00000394236.7:c.1989T>C
|
ENSP00000377783.3:p.Ala663=
|
|
ENST00000407433.5:c.1596T>C
|
ENSP00000385794.1:p.Ala532=
|
|
NM_000313.3:c.1989T>C , LRG_572t1:c.1989T>C
|
NP_000304.2:p.Ala663=
|
|
NM_001314077.1:c.2085T>C , LRG_572t2:c.2085T>C
|
NP_001301006.1:p.Ala695=
|
|
NM_000313.4:c.1989T>C
MANE Select
|
NP_000304.2:p.Ala663=
|
|
NM_001314077.2:c.2085T>C
|
NP_001301006.1:p.Ala695=
|
|