ENST00000348974.5:c.1047G>T
|
ENSP00000330021.7:p.Trp349Cys
|
|
ENST00000394236.9:c.1047G>T
MANE Select
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ENSP00000377783.3:p.Trp349Cys
|
|
ENST00000407433.6:c.1002G>T
|
ENSP00000385794.2:p.Trp334Cys
|
|
ENST00000647936.1:c.1047G>T
|
ENSP00000496822.1:p.Trp349Cys
|
|
ENST00000648381.1:n.1215G>T
|
|
|
ENST00000648853.1:c.1005G>T
|
ENSP00000497262.1:p.Trp335Cys
|
|
ENST00000649103.1:c.1146G>T
|
ENSP00000497962.1:n.1146G>T
|
|
ENST00000650591.1:c.1143G>T
|
ENSP00000497376.1:p.Trp381Cys
|
|
ENST00000394236.7:c.1047G>T
|
ENSP00000377783.3:p.Trp349Cys
|
|
ENST00000407433.5:c.654G>T
|
ENSP00000385794.1:p.Trp218Cys
|
|
NM_000313.3:c.1047G>T , LRG_572t1:c.1047G>T
|
NP_000304.2:p.Trp349Cys
|
|
NM_001314077.1:c.1143G>T , LRG_572t2:c.1143G>T
|
NP_001301006.1:p.Trp381Cys
|
|
NM_000313.4:c.1047G>T
MANE Select
|
NP_000304.2:p.Trp349Cys
|
|
NM_001314077.2:c.1143G>T
|
NP_001301006.1:p.Trp381Cys
|
|