ENST00000367967.8:c.383G>A
|
ENSP00000356944.3:p.Cys128Tyr
|
|
ENST00000426740.8:c.380G>A
|
ENSP00000410180.3:p.Cys127Tyr
|
|
ENST00000436743.7:c.383G>A
|
ENSP00000416607.1:p.Cys128Tyr
|
|
ENST00000442336.2:c.380G>A
|
ENSP00000396567.2:p.Cys127Tyr
|
|
ENST00000699395.1:c.383G>A
|
ENSP00000514356.1:p.Cys128Tyr
|
|
ENST00000699396.1:c.383G>A
|
ENSP00000514357.1:p.Cys128Tyr
|
|
ENST00000699397.1:c.383G>A
|
ENSP00000514358.1:p.Cys128Tyr
|
|
ENST00000699398.1:c.383G>A
|
ENSP00000514359.1:p.Cys128Tyr
|
|
ENST00000699399.1:c.332G>A
|
ENSP00000514360.1:p.Cys111Tyr
|
|
ENST00000699400.1:c.380G>A
|
ENSP00000514361.1:p.Cys127Tyr
|
|
ENST00000699401.1:c.383G>A
|
ENSP00000514362.1:p.Cys128Tyr
|
|
ENST00000699402.1:c.380G>A
|
ENSP00000514363.1:p.Cys127Tyr
|
|
ENST00000699493.1:c.*115G>A
|
ENSP00000514404.1:n.*115G>A
|
|
ENST00000426740.7:c.380G>A
|
ENSP00000410180.3:p.Cys127Tyr
|
|
ENST00000436743.6:c.383G>A
|
ENSP00000416607.1:p.Cys128Tyr
|
|
ENST00000443193.6:c.383G>A
MANE Select
|
ENSP00000392047.2:p.Cys128Tyr
|
|
ENST00000367967.7:c.383G>A
|
ENSP00000356944.3:p.Cys128Tyr
|
|
ENST00000367969.7:c.491G>A
|
ENSP00000356946.3:p.Cys164Tyr
|
|
ENST00000426740.5:c.433G>A
|
|
|
ENST00000436743.5:c.383G>A
|
ENSP00000416607.1:p.Cys128Tyr
|
|
ENST00000443193.5:c.383G>A
|
ENSP00000392047.2:p.Cys128Tyr
|
|
NM_000569.6:c.491G>A
|
NP_000560.5:p.Cys164Tyr
|
|
NM_001127592.1:c.488G>A
|
NP_001121064.1:p.Cys163Tyr
|
|
NM_001127593.1:c.383G>A , LRG_60t1:c.383G>A
|
NP_001121065.1:p.Cys128Tyr
|
|
NM_001127595.1:c.383G>A
|
NP_001121067.1:p.Cys128Tyr
|
|
NM_001127596.1:c.380G>A
|
NP_001121068.1:p.Cys127Tyr
|
|
XM_011509293.1:c.428-1696G>A
|
XP_011507595.1:n.428-1696G>A
|
|
NM_000569.7:c.698G>A
|
NP_000560.6:p.Cys233Tyr
|
|
NM_001127592.2:c.695G>A
|
NP_001121064.2:p.Cys232Tyr
|
|
NM_001329120.1:c.383G>A
|
NP_001316049.1:p.Cys128Tyr
|
|
NM_001329122.1:c.635-1696G>A
|
NP_001316051.1:n.635-1696G>A
|
|
XM_024454064.1:c.380G>A
|
XP_024309832.1:p.Cys127Tyr
|
|
NM_001127595.2:c.383G>A
|
NP_001121067.1:p.Cys128Tyr
|
|
NM_001127596.2:c.380G>A
|
NP_001121068.1:p.Cys127Tyr
|
|
NM_000569.8:c.383G>A
MANE Select
|
NP_000560.7:p.Cys128Tyr
|
|
NM_001329120.2:c.383G>A
|
NP_001316049.1:p.Cys128Tyr
|
|
NM_001386450.1:c.380G>A
|
NP_001373379.1:p.Cys127Tyr
|
|