ENST00000350026.11:c.4991G=
|
ENSP00000055163.8:p.Gly1664=
|
|
ENST00000414678.8:c.5060G=
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ENSP00000412835.3:p.Gly1687=
|
|
ENST00000637015.2:c.5279G=
|
ENSP00000489729.2:p.Gly1760=
|
|
ENST00000346085.10:c.5030G=
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ENSP00000344546.5:p.Gly1677=
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|
ENST00000350026.10:c.4742G=
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ENSP00000055163.7:p.Gly1581=
|
|
ENST00000414678.7:c.3308G=
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ENSP00000412835.2:p.Gly1103=
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|
ENST00000635849.1:c.2471G=
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ENSP00000490948.1:p.Gly824=
|
|
ENST00000635957.1:c.2102G=
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ENSP00000490385.1:p.Gly701=
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ENST00000636227.1:n.3613G=
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|
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ENST00000636254.1:n.1070G=
|
|
|
ENST00000636930.2:c.5150G=
MANE Select
|
ENSP00000490491.2:p.Gly1717=
|
|
ENST00000636940.1:n.3147G=
|
|
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ENST00000637015.1:c.2518G=
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|
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ENST00000637568.1:c.2432G=
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|
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ENST00000637741.1:n.1816G=
|
|
|
ENST00000637810.1:c.2492G=
|
ENSP00000489636.1:p.Gly831=
|
|
ENST00000637904.1:c.2651G=
|
ENSP00000490550.1:p.Gly884=
|
|
ENST00000647938.1:c.4781G=
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ENSP00000498155.1:p.Gly1594=
|
|
ENST00000346085.9:c.4781G=
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ENSP00000344546.4:p.Gly1594=
|
|
ENST00000350026.9:c.4742G=
|
ENSP00000055163.7:p.Gly1581=
|
|
ENST00000414678.6:c.3308G=
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ENSP00000412835.2:p.Gly1103=
|
|
NM_017519.2:c.4742G=
|
NP_059989.2:p.Gly1581=
|
|
NM_020732.3:c.4781G=
|
NP_065783.3:p.Gly1594=
|
|
XM_005267069.3:c.4901G=
|
XP_005267126.2:p.Gly1634=
|
|
XM_011535984.1:c.3980G=
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XP_011534286.1:p.Gly1327=
|
|
XM_011535985.1:c.3800G=
|
XP_011534287.1:p.Gly1267=
|
|
XM_011535986.1:c.3560G=
|
XP_011534288.1:p.Gly1187=
|
|
XM_011535987.1:c.3179G=
|
XP_011534289.1:p.Gly1060=
|
|
XM_011535988.1:c.2042G=
|
XP_011534290.1:p.Gly681=
|
|
NM_001346813.1:c.4901G=
|
NP_001333742.1:p.Gly1634=
|
|
NM_001363725.1:c.2651G=
|
NP_001350654.1:p.Gly884=
|
|
XM_011535984.2:c.5111G=
|
XP_011534286.2:p.Gly1704=
|
|
XM_011535988.3:c.2042G=
|
XP_011534290.1:p.Gly681=
|
|
XM_017011103.2:c.5012G=
|
XP_016866592.1:p.Gly1671=
|
|
XM_017011104.1:c.4982G=
|
XP_016866593.1:p.Gly1661=
|
|
XM_017011105.2:c.4952G=
|
XP_016866594.1:p.Gly1651=
|
|
XM_017011106.2:c.4823G=
|
XP_016866595.1:p.Gly1608=
|
|
XM_017011107.2:c.4802G=
|
XP_016866596.1:p.Gly1601=
|
|
XR_002956289.1:n.5097G=
|
|
|
NM_001363725.2:c.2651G=
|
NP_001350654.1:p.Gly884=
|
|
NM_001371656.1:c.5030G=
|
NP_001358585.1:p.Gly1677=
|
|
NM_001374820.1:c.5030G=
|
NP_001361749.1:p.Gly1677=
|
|
NM_001374828.1:c.5150G=
MANE Select
|
NP_001361757.1:p.Gly1717=
|
|
NM_017519.3:c.4991G=
|
NP_059989.3:p.Gly1664=
|
|