ENST00000370263.9:c.996C>A
MANE Select
|
ENSP00000359285.4:p.His332Gln
|
|
ENST00000370263.8:c.996C>A
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ENSP00000359285.4:p.His332Gln
|
|
ENST00000463705.5:n.1644C>A
|
|
|
ENST00000467563.3:n.1066C>A
|
|
|
ENST00000498043.6:c.1020C>A
|
|
|
ENST00000615287.4:c.783C>A
|
ENSP00000483388.1:p.His261Gln
|
|
ENST00000627000.1:c.*685C>A
|
ENSP00000486914.1:n.*685C>A
|
|
ENST00000630240.1:n.717C>A
|
|
|
NM_000744.6:c.996C>A
|
NP_000735.1:p.His332Gln
|
|
NM_001256573.1:c.468C>A
|
NP_001243502.1:p.His156Gln
|
|
NR_046317.1:n.1252C>A
|
|
|
XM_011528524.1:c.783C>A
|
XP_011526826.1:p.His261Gln
|
|
XM_017027625.2:c.468C>A
|
XP_016883114.1:p.His156Gln
|
|
XM_024451822.1:c.468C>A
|
XP_024307590.1:p.His156Gln
|
|
NM_001256573.2:c.468C>A
|
NP_001243502.1:p.His156Gln
|
|
NR_046317.2:n.1205C>A
|
|
|
NM_000744.7:c.996C>A
MANE Select
|
NP_000735.1:p.His332Gln
|
|