ENST00000350026.11:c.4686C>T
|
ENSP00000055163.8:p.Gly1562=
|
|
ENST00000414678.8:c.4755C>T
|
ENSP00000412835.3:p.Gly1585=
|
|
ENST00000637015.2:c.4974C>T
|
ENSP00000489729.2:p.Gly1658=
|
|
ENST00000346085.10:c.4725C>T
|
ENSP00000344546.5:p.Gly1575=
|
|
ENST00000350026.10:c.4437C>T
|
ENSP00000055163.7:p.Gly1479=
|
|
ENST00000414678.7:c.3003C>T
|
ENSP00000412835.2:p.Gly1001=
|
|
ENST00000635849.1:c.2166C>T
|
ENSP00000490948.1:p.Gly722=
|
|
ENST00000635957.1:c.1797C>T
|
ENSP00000490385.1:p.Gly599=
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ENST00000636227.1:n.3308C>T
|
|
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ENST00000636254.1:n.765C>T
|
|
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ENST00000636930.2:c.4845C>T
MANE Select
|
ENSP00000490491.2:p.Gly1615=
|
|
ENST00000636940.1:n.2842C>T
|
|
|
ENST00000637015.1:c.2213C>T
|
|
|
ENST00000637568.1:c.2127C>T
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|
|
ENST00000637741.1:n.1511C>T
|
|
|
ENST00000637810.1:c.2187C>T
|
ENSP00000489636.1:p.Gly729=
|
|
ENST00000637904.1:c.2346C>T
|
ENSP00000490550.1:p.Gly782=
|
|
ENST00000647938.1:c.4476C>T
|
ENSP00000498155.1:p.Gly1492=
|
|
ENST00000346085.9:c.4476C>T
|
ENSP00000344546.4:p.Gly1492=
|
|
ENST00000350026.9:c.4437C>T
|
ENSP00000055163.7:p.Gly1479=
|
|
ENST00000414678.6:c.3003C>T
|
ENSP00000412835.2:p.Gly1001=
|
|
NM_017519.2:c.4437C>T
|
NP_059989.2:p.Gly1479=
|
|
NM_020732.3:c.4476C>T
|
NP_065783.3:p.Gly1492=
|
|
XM_005267069.3:c.4596C>T
|
XP_005267126.2:p.Gly1532=
|
|
XM_011535984.1:c.3675C>T
|
XP_011534286.1:p.Gly1225=
|
|
XM_011535985.1:c.3495C>T
|
XP_011534287.1:p.Gly1165=
|
|
XM_011535986.1:c.3255C>T
|
XP_011534288.1:p.Gly1085=
|
|
XM_011535987.1:c.2874C>T
|
XP_011534289.1:p.Gly958=
|
|
XM_011535988.1:c.1737C>T
|
XP_011534290.1:p.Gly579=
|
|
NM_001346813.1:c.4596C>T
|
NP_001333742.1:p.Gly1532=
|
|
NM_001363725.1:c.2346C>T
|
NP_001350654.1:p.Gly782=
|
|
XM_011535984.2:c.4806C>T
|
XP_011534286.2:p.Gly1602=
|
|
XM_011535988.3:c.1737C>T
|
XP_011534290.1:p.Gly579=
|
|
XM_017011103.2:c.4707C>T
|
XP_016866592.1:p.Gly1569=
|
|
XM_017011104.1:c.4677C>T
|
XP_016866593.1:p.Gly1559=
|
|
XM_017011105.2:c.4647C>T
|
XP_016866594.1:p.Gly1549=
|
|
XM_017011106.2:c.4518C>T
|
XP_016866595.1:p.Gly1506=
|
|
XM_017011107.2:c.4497C>T
|
XP_016866596.1:p.Gly1499=
|
|
XR_002956289.1:n.4792C>T
|
|
|
NM_001363725.2:c.2346C>T
|
NP_001350654.1:p.Gly782=
|
|
NM_001371656.1:c.4725C>T
|
NP_001358585.1:p.Gly1575=
|
|
NM_001374820.1:c.4725C>T
|
NP_001361749.1:p.Gly1575=
|
|
NM_001374828.1:c.4845C>T
MANE Select
|
NP_001361757.1:p.Gly1615=
|
|
NM_017519.3:c.4686C>T
|
NP_059989.3:p.Gly1562=
|
|