ENST00000456935.7:c.2880G>C
MANE Select
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ENSP00000395473.2:p.Gln960His
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ENST00000221363.8:c.2877G>C
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ENSP00000221363.4:p.Gln959His
|
|
ENST00000456935.6:c.2880G>C
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ENSP00000395473.2:p.Gln960His
|
|
ENST00000466794.5:n.3470G>C
|
|
|
ENST00000469423.1:n.309G>C
|
|
|
ENST00000493218.5:n.291G>C
|
|
|
ENST00000597692.1:c.439G>C
|
|
|
NM_000528.3:c.2880G>C
|
NP_000519.2:p.Gln960His
|
|
NM_001173498.1:c.2877G>C
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NP_001166969.1:p.Gln959His
|
|
XM_005259913.1:c.2883G>C
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XP_005259970.1:p.Gln961His
|
|
XM_011528017.1:c.1779G>C
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XP_011526319.1:p.Gln593His
|
|
XM_005259913.2:c.2883G>C
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XP_005259970.1:p.Gln961His
|
|
XM_024451518.1:c.1779G>C
|
XP_024307286.1:p.Gln593His
|
|
NM_000528.4:c.2880G>C
MANE Select
|
NP_000519.2:p.Gln960His
|
|
NM_001173498.2:c.2877G>C
|
NP_001166969.1:p.Gln959His
|
|