ENST00000262093.11:c.1232G=
MANE Select
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ENSP00000262093.6:p.Cys411=
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ENST00000382873.8:c.1016G=
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ENSP00000372326.4:p.Cys339=
|
|
ENST00000651787.1:n.1338G=
|
|
|
ENST00000652755.1:c.1250G=
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ENSP00000498358.1:p.Cys417=
|
|
ENST00000262093.9:c.1232G=
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ENSP00000262093.5:p.Cys411=
|
|
ENST00000382873.7:c.1250G=
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ENSP00000372326.3:p.Cys417=
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|
ENST00000585494.5:c.*959G=
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ENSP00000465243.1:n.*959G=
|
|
NM_000140.3:c.1232G=
|
NP_000131.2:p.Cys411=
|
|
NM_001012515.2:c.1250G=
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NP_001012533.1:p.Cys417=
|
|
XM_011525881.1:c.1151G=
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XP_011524183.1:p.Cys384=
|
|
XM_011525882.1:c.1016G=
|
XP_011524184.1:p.Cys339=
|
|
NM_000140.4:c.1232G=
|
NP_000131.2:p.Cys411=
|
|
NM_001012515.3:c.1250G=
|
NP_001012533.1:p.Cys417=
|
|
XM_011525882.2:c.1016G=
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XP_011524184.1:p.Cys339=
|
|
XM_017025614.2:c.1133G=
|
XP_016881103.1:p.Cys378=
|
|
NM_000140.5:c.1232G=
MANE Select
|
NP_000131.2:p.Cys411=
|
|
NM_001012515.4:c.1250G=
|
NP_001012533.1:p.Cys417=
|
|
NM_001371094.1:c.1133G=
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NP_001358023.1:p.Cys378=
|
|
NM_001371095.1:c.1016G=
|
NP_001358024.1:p.Cys339=
|
|
NM_001374778.1:c.1172G=
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NP_001361707.1:p.Cys391=
|
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