ENST00000224721.12:c.6978C=
MANE Select
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ENSP00000224721.9:p.Gly2326=
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ENST00000642965.1:c.911C=
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ENSP00000495222.1:n.911C=
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|
ENST00000647092.1:c.575C=
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ENSP00000495176.1:n.575C=
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ENST00000224721.10:c.6993C=
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ENSP00000224721.8:p.Gly2331=
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ENST00000398788.4:c.258C=
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ENSP00000381768.3:p.Gly86=
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ENST00000475158.1:n.514C=
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|
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ENST00000619887.4:c.258C=
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ENSP00000478374.1:p.Gly86=
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|
ENST00000622827.4:c.6978C=
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ENSP00000483211.1:p.Gly2326=
|
|
NM_001171933.1:c.258C=
|
NP_001165404.1:p.Gly86=
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NM_001171934.1:c.258C=
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NP_001165405.1:p.Gly86=
|
|
NM_022124.5:c.6978C=
|
NP_071407.4:p.Gly2326=
|
|
XM_006717940.2:c.7173C=
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XP_006718003.1:p.Gly2391=
|
|
XM_006717942.2:c.7107C=
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XP_006718005.1:p.Gly2369=
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XM_011540039.1:c.7170C=
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XP_011538341.1:p.Gly2390=
|
|
XM_011540040.1:c.7167C=
|
XP_011538342.1:p.Gly2389=
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|
XM_011540041.1:c.7113C=
|
XP_011538343.1:p.Gly2371=
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|
XM_011540042.1:c.7083C=
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XP_011538344.1:p.Gly2361=
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|
XM_011540043.1:c.7173C=
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XP_011538345.1:p.Gly2391=
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|
XM_011540044.1:c.7038C=
|
XP_011538346.1:p.Gly2346=
|
|
XM_011540045.1:c.7173C=
|
XP_011538347.1:p.Gly2391=
|
|
XM_011540046.1:c.6633C=
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XP_011538348.1:p.Gly2211=
|
|
XM_011540047.1:c.5991C=
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XP_011538349.1:p.Gly1997=
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XM_011540052.1:c.3501C=
|
XP_011538354.1:p.Gly1167=
|
|
NM_022124.6:c.6978C=
MANE Select
|
NP_071407.4:p.Gly2326=
|
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