ENST00000348974.5:c.683G>A
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ENSP00000330021.7:p.Cys228Tyr
|
|
ENST00000394236.9:c.683G>A
MANE Select
|
ENSP00000377783.3:p.Cys228Tyr
|
|
ENST00000407433.6:c.638G>A
|
ENSP00000385794.2:p.Cys213Tyr
|
|
ENST00000647936.1:c.683G>A
|
ENSP00000496822.1:p.Cys228Tyr
|
|
ENST00000648381.1:n.851G>A
|
|
|
ENST00000648853.1:c.641G>A
|
ENSP00000497262.1:p.Cys214Tyr
|
|
ENST00000649103.1:c.782G>A
|
ENSP00000497962.1:n.782G>A
|
|
ENST00000650591.1:c.779G>A
|
ENSP00000497376.1:p.Cys260Tyr
|
|
ENST00000394236.7:c.683G>A
|
ENSP00000377783.3:p.Cys228Tyr
|
|
ENST00000407433.5:c.290G>A
|
ENSP00000385794.1:p.Cys97Tyr
|
|
NM_000313.3:c.683G>A , LRG_572t1:c.683G>A
|
NP_000304.2:p.Cys228Tyr
|
|
NM_001314077.1:c.779G>A , LRG_572t2:c.779G>A
|
NP_001301006.1:p.Cys260Tyr
|
|
NM_000313.4:c.683G>A
MANE Select
|
NP_000304.2:p.Cys228Tyr
|
|
NM_001314077.2:c.779G>A
|
NP_001301006.1:p.Cys260Tyr
|
|