ENST00000370263.9:c.1061G=
MANE Select
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ENSP00000359285.4:p.Arg354=
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ENST00000370263.8:c.1061G=
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ENSP00000359285.4:p.Arg354=
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ENST00000463705.5:n.1709G=
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|
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ENST00000467563.3:n.1131G=
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|
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ENST00000498043.6:c.1085G=
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|
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ENST00000615287.4:c.848G=
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ENSP00000483388.1:p.Arg283=
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ENST00000627000.1:c.*750G=
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ENSP00000486914.1:n.*750G=
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ENST00000630240.1:n.782G=
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|
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NM_000744.6:c.1061G=
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NP_000735.1:p.Arg354=
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NM_001256573.1:c.533G=
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NP_001243502.1:p.Arg178=
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NR_046317.1:n.1317G=
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|
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XM_011528524.1:c.848G=
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XP_011526826.1:p.Arg283=
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|
XM_017027625.2:c.533G=
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XP_016883114.1:p.Arg178=
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|
XM_024451822.1:c.533G=
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XP_024307590.1:p.Arg178=
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|
NM_001256573.2:c.533G=
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NP_001243502.1:p.Arg178=
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|
NR_046317.2:n.1270G=
|
|
|
NM_000744.7:c.1061G=
MANE Select
|
NP_000735.1:p.Arg354=
|
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