ENST00000350026.11:c.4684G=
|
ENSP00000055163.8:p.Gly1562=
|
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ENST00000414678.8:c.4753G=
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ENSP00000412835.3:p.Gly1585=
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ENST00000637015.2:c.4972G=
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ENSP00000489729.2:p.Gly1658=
|
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ENST00000346085.10:c.4723G=
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ENSP00000344546.5:p.Gly1575=
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ENST00000350026.10:c.4435G=
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ENSP00000055163.7:p.Gly1479=
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ENST00000414678.7:c.3001G=
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ENSP00000412835.2:p.Gly1001=
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|
ENST00000635849.1:c.2164G=
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ENSP00000490948.1:p.Gly722=
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|
ENST00000635957.1:c.1795G=
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ENSP00000490385.1:p.Gly599=
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ENST00000636227.1:n.3306G=
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|
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ENST00000636254.1:n.763G=
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|
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ENST00000636930.2:c.4843G=
MANE Select
|
ENSP00000490491.2:p.Gly1615=
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ENST00000636940.1:n.2840G=
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|
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ENST00000637015.1:c.2211G=
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|
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ENST00000637568.1:c.2125G=
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|
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ENST00000637741.1:n.1509G=
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|
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ENST00000637810.1:c.2185G=
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ENSP00000489636.1:p.Gly729=
|
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ENST00000637904.1:c.2344G=
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ENSP00000490550.1:p.Gly782=
|
|
ENST00000647938.1:c.4474G=
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ENSP00000498155.1:p.Gly1492=
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|
ENST00000346085.9:c.4474G=
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ENSP00000344546.4:p.Gly1492=
|
|
ENST00000350026.9:c.4435G=
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ENSP00000055163.7:p.Gly1479=
|
|
ENST00000414678.6:c.3001G=
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ENSP00000412835.2:p.Gly1001=
|
|
NM_017519.2:c.4435G=
|
NP_059989.2:p.Gly1479=
|
|
NM_020732.3:c.4474G=
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NP_065783.3:p.Gly1492=
|
|
XM_005267069.3:c.4594G=
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XP_005267126.2:p.Gly1532=
|
|
XM_011535984.1:c.3673G=
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XP_011534286.1:p.Gly1225=
|
|
XM_011535985.1:c.3493G=
|
XP_011534287.1:p.Gly1165=
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|
XM_011535986.1:c.3253G=
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XP_011534288.1:p.Gly1085=
|
|
XM_011535987.1:c.2872G=
|
XP_011534289.1:p.Gly958=
|
|
XM_011535988.1:c.1735G=
|
XP_011534290.1:p.Gly579=
|
|
NM_001346813.1:c.4594G=
|
NP_001333742.1:p.Gly1532=
|
|
NM_001363725.1:c.2344G=
|
NP_001350654.1:p.Gly782=
|
|
XM_011535984.2:c.4804G=
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XP_011534286.2:p.Gly1602=
|
|
XM_011535988.3:c.1735G=
|
XP_011534290.1:p.Gly579=
|
|
XM_017011103.2:c.4705G=
|
XP_016866592.1:p.Gly1569=
|
|
XM_017011104.1:c.4675G=
|
XP_016866593.1:p.Gly1559=
|
|
XM_017011105.2:c.4645G=
|
XP_016866594.1:p.Gly1549=
|
|
XM_017011106.2:c.4516G=
|
XP_016866595.1:p.Gly1506=
|
|
XM_017011107.2:c.4495G=
|
XP_016866596.1:p.Gly1499=
|
|
XR_002956289.1:n.4790G=
|
|
|
NM_001363725.2:c.2344G=
|
NP_001350654.1:p.Gly782=
|
|
NM_001371656.1:c.4723G=
|
NP_001358585.1:p.Gly1575=
|
|
NM_001374820.1:c.4723G=
|
NP_001361749.1:p.Gly1575=
|
|
NM_001374828.1:c.4843G=
MANE Select
|
NP_001361757.1:p.Gly1615=
|
|
NM_017519.3:c.4684G=
|
NP_059989.3:p.Gly1562=
|
|