ENST00000222214.10:c.344G=
MANE Select
|
ENSP00000222214.4:p.Cys115=
|
|
ENST00000222214.9:c.344G=
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ENSP00000222214.4:p.Cys115=
|
|
ENST00000421816.6:n.322G=
|
|
|
ENST00000585420.5:n.709G=
|
|
|
ENST00000587072.1:c.392G=
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ENSP00000468584.1:p.Cys131=
|
|
ENST00000587832.5:n.401G=
|
|
|
ENST00000588905.5:c.308G=
|
ENSP00000465770.1:p.Cys103=
|
|
ENST00000589039.5:c.281G=
|
ENSP00000465618.1:p.Cys94=
|
|
ENST00000590530.5:c.399G=
|
ENSP00000468452.1:p.Leu133=
|
|
ENST00000590627.5:n.709G=
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|
|
ENST00000591043.1:n.380G=
|
|
|
ENST00000591470.5:c.344G=
|
ENSP00000466845.1:p.Cys115=
|
|
NM_000159.3:c.344G=
|
NP_000150.1:p.Cys115=
|
|
NM_013976.3:c.344G=
|
NP_039663.1:p.Cys115=
|
|
NR_102316.1:n.507G=
|
|
|
NR_102317.1:n.760G=
|
|
|
XM_006722721.2:c.344G=
|
XP_006722784.1:p.Cys115=
|
|
XM_011527899.1:c.344G=
|
XP_011526201.1:p.Cys115=
|
|
XM_011527900.1:c.344G=
|
XP_011526202.1:p.Cys115=
|
|
XM_011527899.2:c.344G=
|
XP_011526201.1:p.Cys115=
|
|
XM_011527900.2:c.344G=
|
XP_011526202.1:p.Cys115=
|
|
XM_017026580.1:c.344G=
|
XP_016882069.1:p.Cys115=
|
|
NM_000159.4:c.344G=
MANE Select
|
NP_000150.1:p.Cys115=
|
|
NM_013976.4:c.344G=
|
NP_039663.1:p.Cys115=
|
|
NM_013976.5:c.344G=
|
NP_039663.1:p.Cys115=
|
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