ENST00000330889.8:c.898G>A
MANE Select
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ENSP00000329468.3:p.Gly300Ser
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ENST00000330889.7:c.898G>A
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ENSP00000329468.3:p.Gly300Ser
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ENST00000470962.1:n.318G>A
|
|
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ENST00000480980.1:n.332G>A
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|
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ENST00000580525.5:c.916G>A
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ENSP00000464121.1:p.Gly306Ser
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ENST00000581285.5:c.814G>A
|
ENSP00000464155.1:p.Gly272Ser
|
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ENST00000584828.5:c.267G>A
|
|
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ENST00000584989.1:c.190G>A
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ENSP00000462634.1:p.Gly64Ser
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ENST00000585130.5:c.*497G>A
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ENSP00000464120.1:n.*497G>A
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NM_018404.2:c.898G>A
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NP_060874.1:p.Gly300Ser
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XM_005258008.2:c.916G>A
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XP_005258065.1:p.Gly306Ser
|
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XM_005258011.2:c.853G>A
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XP_005258068.1:p.Gly285Ser
|
|
XM_006721973.2:c.916G>A
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XP_006722036.1:p.Gly306Ser
|
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XM_011524993.1:c.913G>A
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XP_011523295.1:p.Gly305Ser
|
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XM_011524994.1:c.895G>A
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XP_011523296.1:p.Gly299Ser
|
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NM_001346712.1:c.916G>A
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NP_001333641.1:p.Gly306Ser
|
|
NM_001346714.1:c.895G>A
|
NP_001333643.1:p.Gly299Ser
|
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NM_001346716.1:c.898G>A
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NP_001333645.1:p.Gly300Ser
|
|
NR_144488.1:n.1097G>A
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|
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XM_024450831.1:c.898G>A
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XP_024306599.1:p.Gly300Ser
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XM_024450832.1:c.913G>A
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XP_024306600.1:p.Gly305Ser
|
|
XM_024450833.1:c.853G>A
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XP_024306601.1:p.Gly285Ser
|
|
XM_024450834.1:c.916G>A
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XP_024306602.1:p.Gly306Ser
|
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XM_024450835.1:c.532G>A
|
XP_024306603.1:p.Gly178Ser
|
|
NM_018404.3:c.898G>A
MANE Select
|
NP_060874.1:p.Gly300Ser
|
|
NM_001346712.2:c.916G>A
|
NP_001333641.1:p.Gly306Ser
|
|
NM_001346714.2:c.895G>A
|
NP_001333643.1:p.Gly299Ser
|
|
NM_001346716.2:c.898G>A
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NP_001333645.1:p.Gly300Ser
|
|
NR_144488.2:n.888G>A
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