ENST00000348974.5:c.801T>G
|
ENSP00000330021.7:p.Cys267Trp
|
|
ENST00000394236.9:c.801T>G
MANE Select
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ENSP00000377783.3:p.Cys267Trp
|
|
ENST00000407433.6:c.756T>G
|
ENSP00000385794.2:p.Cys252Trp
|
|
ENST00000647936.1:c.801T>G
|
ENSP00000496822.1:p.Cys267Trp
|
|
ENST00000648381.1:n.969T>G
|
|
|
ENST00000648853.1:c.759T>G
|
ENSP00000497262.1:p.Cys253Trp
|
|
ENST00000649103.1:c.900T>G
|
ENSP00000497962.1:n.900T>G
|
|
ENST00000650591.1:c.897T>G
|
ENSP00000497376.1:p.Cys299Trp
|
|
ENST00000394236.7:c.801T>G
|
ENSP00000377783.3:p.Cys267Trp
|
|
ENST00000407433.5:c.408T>G
|
ENSP00000385794.1:p.Cys136Trp
|
|
NM_000313.3:c.801T>G , LRG_572t1:c.801T>G
|
NP_000304.2:p.Cys267Trp
|
|
NM_001314077.1:c.897T>G , LRG_572t2:c.897T>G
|
NP_001301006.1:p.Cys299Trp
|
|
NM_000313.4:c.801T>G
MANE Select
|
NP_000304.2:p.Cys267Trp
|
|
NM_001314077.2:c.897T>G
|
NP_001301006.1:p.Cys299Trp
|
|