ENST00000350026.11:c.4655G=
|
ENSP00000055163.8:p.Gly1552=
|
|
ENST00000414678.8:c.4724G=
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ENSP00000412835.3:p.Gly1575=
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|
ENST00000637015.2:c.4943G=
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ENSP00000489729.2:p.Gly1648=
|
|
ENST00000346085.10:c.4694G=
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ENSP00000344546.5:p.Gly1565=
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|
ENST00000350026.10:c.4406G=
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ENSP00000055163.7:p.Gly1469=
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|
ENST00000414678.7:c.2972G=
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ENSP00000412835.2:p.Gly991=
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|
ENST00000635849.1:c.2135G=
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ENSP00000490948.1:p.Gly712=
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|
ENST00000635957.1:c.1766G=
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ENSP00000490385.1:p.Gly589=
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ENST00000636227.1:n.3277G=
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|
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ENST00000636254.1:n.734G=
|
|
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ENST00000636930.2:c.4814G=
MANE Select
|
ENSP00000490491.2:p.Gly1605=
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|
ENST00000636940.1:n.2811G=
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|
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ENST00000637015.1:c.2182G=
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|
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ENST00000637568.1:c.2096G=
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|
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ENST00000637741.1:n.1480G=
|
|
|
ENST00000637810.1:c.2156G=
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ENSP00000489636.1:p.Gly719=
|
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ENST00000637904.1:c.2315G=
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ENSP00000490550.1:p.Gly772=
|
|
ENST00000647938.1:c.4445G=
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ENSP00000498155.1:p.Gly1482=
|
|
ENST00000346085.9:c.4445G=
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ENSP00000344546.4:p.Gly1482=
|
|
ENST00000350026.9:c.4406G=
|
ENSP00000055163.7:p.Gly1469=
|
|
ENST00000414678.6:c.2972G=
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ENSP00000412835.2:p.Gly991=
|
|
NM_017519.2:c.4406G=
|
NP_059989.2:p.Gly1469=
|
|
NM_020732.3:c.4445G=
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NP_065783.3:p.Gly1482=
|
|
XM_005267069.3:c.4565G=
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XP_005267126.2:p.Gly1522=
|
|
XM_011535984.1:c.3644G=
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XP_011534286.1:p.Gly1215=
|
|
XM_011535985.1:c.3464G=
|
XP_011534287.1:p.Gly1155=
|
|
XM_011535986.1:c.3224G=
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XP_011534288.1:p.Gly1075=
|
|
XM_011535987.1:c.2843G=
|
XP_011534289.1:p.Gly948=
|
|
XM_011535988.1:c.1706G=
|
XP_011534290.1:p.Gly569=
|
|
NM_001346813.1:c.4565G=
|
NP_001333742.1:p.Gly1522=
|
|
NM_001363725.1:c.2315G=
|
NP_001350654.1:p.Gly772=
|
|
XM_011535984.2:c.4775G=
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XP_011534286.2:p.Gly1592=
|
|
XM_011535988.3:c.1706G=
|
XP_011534290.1:p.Gly569=
|
|
XM_017011103.2:c.4676G=
|
XP_016866592.1:p.Gly1559=
|
|
XM_017011104.1:c.4646G=
|
XP_016866593.1:p.Gly1549=
|
|
XM_017011105.2:c.4616G=
|
XP_016866594.1:p.Gly1539=
|
|
XM_017011106.2:c.4487G=
|
XP_016866595.1:p.Gly1496=
|
|
XM_017011107.2:c.4466G=
|
XP_016866596.1:p.Gly1489=
|
|
XR_002956289.1:n.4761G=
|
|
|
NM_001363725.2:c.2315G=
|
NP_001350654.1:p.Gly772=
|
|
NM_001371656.1:c.4694G=
|
NP_001358585.1:p.Gly1565=
|
|
NM_001374820.1:c.4694G=
|
NP_001361749.1:p.Gly1565=
|
|
NM_001374828.1:c.4814G=
MANE Select
|
NP_001361757.1:p.Gly1605=
|
|
NM_017519.3:c.4655G=
|
NP_059989.3:p.Gly1552=
|
|