ENST00000456935.7:c.2678G>A
MANE Select
|
ENSP00000395473.2:p.Arg893His
|
|
ENST00000221363.8:c.2675G>A
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ENSP00000221363.4:p.Arg892His
|
|
ENST00000456935.6:c.2678G>A
|
ENSP00000395473.2:p.Arg893His
|
|
ENST00000466794.5:n.3268G>A
|
|
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ENST00000493218.5:n.89G>A
|
|
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ENST00000597692.1:c.237G>A
|
|
|
NM_000528.3:c.2678G>A
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NP_000519.2:p.Arg893His
|
|
NM_001173498.1:c.2675G>A
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NP_001166969.1:p.Arg892His
|
|
XM_005259913.1:c.2681G>A
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XP_005259970.1:p.Arg894His
|
|
XM_011528017.1:c.1577G>A
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XP_011526319.1:p.Arg526His
|
|
XM_005259913.2:c.2681G>A
|
XP_005259970.1:p.Arg894His
|
|
XM_024451518.1:c.1577G>A
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XP_024307286.1:p.Arg526His
|
|
NM_000528.4:c.2678G>A
MANE Select
|
NP_000519.2:p.Arg893His
|
|
NM_001173498.2:c.2675G>A
|
NP_001166969.1:p.Arg892His
|
|