ENST00000348974.5:c.777C>G
|
ENSP00000330021.7:p.Tyr259Ter
|
|
ENST00000394236.9:c.777C>G
MANE Select
|
ENSP00000377783.3:p.Tyr259Ter
|
|
ENST00000407433.6:c.732C>G
|
ENSP00000385794.2:p.Tyr244Ter
|
|
ENST00000647936.1:c.777C>G
|
ENSP00000496822.1:p.Tyr259Ter
|
|
ENST00000648381.1:n.945C>G
|
|
|
ENST00000648853.1:c.735C>G
|
ENSP00000497262.1:p.Tyr245Ter
|
|
ENST00000649103.1:c.876C>G
|
ENSP00000497962.1:n.876C>G
|
|
ENST00000650591.1:c.873C>G
|
ENSP00000497376.1:p.Tyr291Ter
|
|
ENST00000394236.7:c.777C>G
|
ENSP00000377783.3:p.Tyr259Ter
|
|
ENST00000407433.5:c.384C>G
|
ENSP00000385794.1:p.Tyr128Ter
|
|
NM_000313.3:c.777C>G , LRG_572t1:c.777C>G
|
NP_000304.2:p.Tyr259Ter
|
|
NM_001314077.1:c.873C>G , LRG_572t2:c.873C>G
|
NP_001301006.1:p.Tyr291Ter
|
|
NM_000313.4:c.777C>G
MANE Select
|
NP_000304.2:p.Tyr259Ter
|
|
NM_001314077.2:c.873C>G
|
NP_001301006.1:p.Tyr291Ter
|
|