ENST00000348974.5:c.835C>T
|
ENSP00000330021.7:p.Gln279Ter
|
|
ENST00000394236.9:c.835C>T
MANE Select
|
ENSP00000377783.3:p.Gln279Ter
|
|
ENST00000407433.6:c.790C>T
|
ENSP00000385794.2:p.Gln264Ter
|
|
ENST00000647936.1:c.835C>T
|
ENSP00000496822.1:p.Gln279Ter
|
|
ENST00000648381.1:n.1003C>T
|
|
|
ENST00000648853.1:c.793C>T
|
ENSP00000497262.1:p.Gln265Ter
|
|
ENST00000649103.1:c.934C>T
|
ENSP00000497962.1:n.934C>T
|
|
ENST00000650591.1:c.931C>T
|
ENSP00000497376.1:p.Gln311Ter
|
|
ENST00000394236.7:c.835C>T
|
ENSP00000377783.3:p.Gln279Ter
|
|
ENST00000407433.5:c.442C>T
|
ENSP00000385794.1:p.Gln148Ter
|
|
NM_000313.3:c.835C>T , LRG_572t1:c.835C>T
|
NP_000304.2:p.Gln279Ter
|
|
NM_001314077.1:c.931C>T , LRG_572t2:c.931C>T
|
NP_001301006.1:p.Gln311Ter
|
|
NM_000313.4:c.835C>T
MANE Select
|
NP_000304.2:p.Gln279Ter
|
|
NM_001314077.2:c.931C>T
|
NP_001301006.1:p.Gln311Ter
|
|