ENST00000377443.7:c.375G>A
MANE Select
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ENSP00000366662.2:p.Glu125=
|
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ENST00000377436.6:c.375G>A
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ENSP00000366654.3:p.Glu125=
|
|
ENST00000377442.3:c.195G>A
|
ENSP00000366661.2:p.Glu65=
|
|
ENST00000377443.6:c.375G>A
|
ENSP00000366662.2:p.Glu125=
|
|
ENST00000476083.1:n.99-1658G>A
|
|
|
ENST00000549778.5:c.279G>A
|
ENSP00000447108.1:p.Glu93=
|
|
NM_001215.3:c.375G>A
|
NP_001206.2:p.Glu125=
|
|
NM_001270500.1:c.375G>A
|
NP_001257429.1:p.Glu125=
|
|
NM_001270501.1:c.195G>A
|
NP_001257430.1:p.Glu65=
|
|
NM_001270502.1:c.25-1658G>A
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NP_001257431.1:n.25-1658G>A
|
|
XM_011542083.1:c.387G>A
|
XP_011540385.1:p.Glu129=
|
|
XM_011542084.1:c.387G>A
|
XP_011540386.1:p.Glu129=
|
|
XM_011542083.3:c.387G>A
|
XP_011540385.1:p.Glu129=
|
|
XM_011542084.3:c.387G>A
|
XP_011540386.1:p.Glu129=
|
|
NM_001215.4:c.375G>A
MANE Select
|
NP_001206.2:p.Glu125=
|
|
NM_001270500.2:c.375G>A
|
NP_001257429.1:p.Glu125=
|
|
NM_001270501.2:c.195G>A
|
NP_001257430.1:p.Glu65=
|
|
NM_001270502.2:c.25-1658G>A
|
NP_001257431.1:n.25-1658G>A
|
|