ENST00000348974.5:c.701A>G
|
ENSP00000330021.7:p.Tyr234Cys
|
|
ENST00000394236.9:c.701A>G
MANE Select
|
ENSP00000377783.3:p.Tyr234Cys
|
|
ENST00000407433.6:c.656A>G
|
ENSP00000385794.2:p.Tyr219Cys
|
|
ENST00000647936.1:c.701A>G
|
ENSP00000496822.1:p.Tyr234Cys
|
|
ENST00000648381.1:n.869A>G
|
|
|
ENST00000648853.1:c.659A>G
|
ENSP00000497262.1:p.Tyr220Cys
|
|
ENST00000649103.1:c.800A>G
|
ENSP00000497962.1:n.800A>G
|
|
ENST00000650591.1:c.797A>G
|
ENSP00000497376.1:p.Tyr266Cys
|
|
ENST00000394236.7:c.701A>G
|
ENSP00000377783.3:p.Tyr234Cys
|
|
ENST00000407433.5:c.308A>G
|
ENSP00000385794.1:p.Tyr103Cys
|
|
NM_000313.3:c.701A>G , LRG_572t1:c.701A>G
|
NP_000304.2:p.Tyr234Cys
|
|
NM_001314077.1:c.797A>G , LRG_572t2:c.797A>G
|
NP_001301006.1:p.Tyr266Cys
|
|
NM_000313.4:c.701A>G
MANE Select
|
NP_000304.2:p.Tyr234Cys
|
|
NM_001314077.2:c.797A>G
|
NP_001301006.1:p.Tyr266Cys
|
|