ENST00000348974.5:c.789C>A
|
ENSP00000330021.7:p.Tyr263Ter
|
|
ENST00000394236.9:c.789C>A
MANE Select
|
ENSP00000377783.3:p.Tyr263Ter
|
|
ENST00000407433.6:c.744C>A
|
ENSP00000385794.2:p.Tyr248Ter
|
|
ENST00000647936.1:c.789C>A
|
ENSP00000496822.1:p.Tyr263Ter
|
|
ENST00000648381.1:n.957C>A
|
|
|
ENST00000648853.1:c.747C>A
|
ENSP00000497262.1:p.Tyr249Ter
|
|
ENST00000649103.1:c.888C>A
|
ENSP00000497962.1:n.888C>A
|
|
ENST00000650591.1:c.885C>A
|
ENSP00000497376.1:p.Tyr295Ter
|
|
ENST00000394236.7:c.789C>A
|
ENSP00000377783.3:p.Tyr263Ter
|
|
ENST00000407433.5:c.396C>A
|
ENSP00000385794.1:p.Tyr132Ter
|
|
NM_000313.3:c.789C>A , LRG_572t1:c.789C>A
|
NP_000304.2:p.Tyr263Ter
|
|
NM_001314077.1:c.885C>A , LRG_572t2:c.885C>A
|
NP_001301006.1:p.Tyr295Ter
|
|
NM_000313.4:c.789C>A
MANE Select
|
NP_000304.2:p.Tyr263Ter
|
|
NM_001314077.2:c.885C>A
|
NP_001301006.1:p.Tyr295Ter
|
|