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ENST00000356839.10:c.673G=
MANE Select
|
ENSP00000349297.5:p.Ala225=
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|
|
ENST00000322910.9:c.*628G=
|
ENSP00000325395.5:n.*628G=
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|
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ENST00000350303.9:c.607G=
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ENSP00000344152.5:p.Ala203=
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|
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ENST00000356839.9:c.673G=
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ENSP00000349297.5:p.Ala225=
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|
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ENST00000543245.6:c.742G=
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ENSP00000438689.2:p.Ala248=
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|
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ENST00000577191.5:n.750G=
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|
|
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ENST00000577857.5:n.489G=
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|
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ENST00000579286.5:n.854G=
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|
|
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ENST00000580365.1:n.404G=
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|
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ENST00000581378.5:c.391G=
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ENST00000582379.1:n.57G=
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|
|
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ENST00000583760.1:n.455G=
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|
|
|
NM_000018.3:c.673G=
|
NP_000009.1:p.Ala225=
|
|
|
NM_001033859.2:c.607G=
|
NP_001029031.1:p.Ala203=
|
|
|
NM_001270447.1:c.742G=
|
NP_001257376.1:p.Ala248=
|
|
|
NM_001270448.1:c.445G=
|
NP_001257377.1:p.Ala149=
|
|
|
XM_006721516.2:c.673G=
|
XP_006721579.2:p.Ala225=
|
|
|
XM_011523829.1:c.673G=
|
XP_011522131.1:p.Ala225=
|
|
|
XM_011523830.1:c.673G=
|
XP_011522132.1:p.Ala225=
|
|
|
XR_934021.1:n.780G=
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XR_934022.1:n.780G=
|
|
|
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XR_934023.1:n.780G=
|
|
|
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XM_006721516.3:c.673G=
|
XP_006721579.2:p.Ala225=
|
|
|
XM_011523829.2:c.673G=
|
XP_011522131.1:p.Ala225=
|
|
|
XM_011523830.2:c.673G=
|
XP_011522132.1:p.Ala225=
|
|
|
XM_024450741.1:c.673G=
|
XP_024306509.1:p.Ala225=
|
|
|
XR_934021.2:n.732G=
|
|
|
|
XR_934022.2:n.732G=
|
|
|
|
XR_934023.2:n.732G=
|
|
|
|
NM_000018.4:c.673G=
MANE Select
|
NP_000009.1:p.Ala225=
|
|
|
NM_001033859.3:c.607G=
|
NP_001029031.1:p.Ala203=
|
|
|
NM_001270447.2:c.742G=
|
NP_001257376.1:p.Ala248=
|
|
|
NM_001270448.2:c.445G=
|
NP_001257377.1:p.Ala149=
|
|
