ENST00000446859.7:c.908G>A
MANE Select
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ENSP00000414635.1:p.Cys303Tyr
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|
ENST00000446859.5:c.908G>A
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ENSP00000414635.1:p.Cys303Tyr
|
|
ENST00000522080.5:n.885G>A
|
|
|
ENST00000522329.1:n.157G>A
|
|
|
ENST00000522526.6:c.812G>A
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ENSP00000429278.2:p.Cys271Tyr
|
|
ENST00000522596.6:n.890G>A
|
|
|
ENST00000522830.5:c.725G>A
|
ENSP00000429593.1:p.Cys242Tyr
|
|
ENST00000524054.5:n.756G>A
|
|
|
ENST00000524327.5:n.708G>A
|
|
|
ENST00000528597.1:c.155G>A
|
ENSP00000436883.1:p.Trp52Ter
|
|
ENST00000602774.1:n.294G>A
|
|
|
NM_001172779.1:c.908G>A
|
NP_001166250.1:p.Cys303Tyr
|
|
NM_001172780.1:c.908G>A
|
NP_001166251.1:p.Cys303Tyr
|
|
NM_153353.4:c.812G>A
|
NP_699184.2:p.Cys271Tyr
|
|
XM_005247133.2:c.725G>A
|
XP_005247190.1:p.Cys242Tyr
|
|
XM_006713508.2:c.854G>A
|
XP_006713571.1:p.Cys285Tyr
|
|
XM_011512442.1:c.905G>A
|
XP_011510744.1:p.Cys302Tyr
|
|
NM_001363888.1:c.725G>A
|
NP_001350817.1:p.Cys242Tyr
|
|
XM_006713508.4:c.854G>A
|
XP_006713571.1:p.Cys285Tyr
|
|
XM_011512442.2:c.905G>A
|
XP_011510744.1:p.Cys302Tyr
|
|
XM_017005746.1:c.722G>A
|
XP_016861235.1:p.Cys241Tyr
|
|
NM_001172779.2:c.908G>A
MANE Select
|
NP_001166250.1:p.Cys303Tyr
|
|
NM_001172780.2:c.908G>A
|
NP_001166251.1:p.Cys303Tyr
|
|
NM_001363888.2:c.725G>A
|
NP_001350817.1:p.Cys242Tyr
|
|
NM_001370608.1:c.722G>A
|
NP_001357537.1:p.Cys241Tyr
|
|
NM_001370609.1:c.725G>A
|
NP_001357538.1:p.Cys242Tyr
|
|
NM_153353.5:c.812G>A
|
NP_699184.2:p.Cys271Tyr
|
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