ENST00000392666.6:c.566G>A
MANE Select
|
ENSP00000376434.1:p.Cys189Tyr
|
|
ENST00000324036.7:c.566G>A
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ENSP00000316233.3:p.Cys189Tyr
|
|
ENST00000392664.2:c.623G>A
|
ENSP00000376432.2:p.Cys208Tyr
|
|
ENST00000392665.6:c.566G>A
|
ENSP00000376433.2:p.Cys189Tyr
|
|
ENST00000392666.5:c.566G>A
|
ENSP00000376434.1:p.Cys189Tyr
|
|
ENST00000440599.6:c.566G>A
|
ENSP00000406320.2:p.Cys189Tyr
|
|
NM_000220.4:c.623G>A
|
NP_000211.1:p.Cys208Tyr
|
|
NM_153764.2:c.566G>A
|
NP_722448.1:p.Cys189Tyr
|
|
NM_153765.2:c.617G>A
|
NP_722449.3:p.Cys206Tyr
|
|
NM_153766.2:c.566G>A
|
NP_722450.1:p.Cys189Tyr
|
|
NM_153767.3:c.566G>A
|
NP_722451.1:p.Cys189Tyr
|
|
NM_000220.6:c.623G>A
|
NP_000211.1:p.Cys208Tyr
|
|
NM_153764.3:c.566G>A
|
NP_722448.1:p.Cys189Tyr
|
|
NM_153765.3:c.617G>A
|
NP_722449.3:p.Cys206Tyr
|
|
NM_153766.3:c.566G>A
MANE Select
|
NP_722450.1:p.Cys189Tyr
|
|
NM_153767.4:c.566G>A
|
NP_722451.1:p.Cys189Tyr
|
|