ENST00000302068.9:c.1131A>G
MANE Select
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ENSP00000306099.4:p.Gly377=
|
|
ENST00000302068.8:c.1131A>G
|
ENSP00000306099.4:p.Gly377=
|
|
ENST00000502545.5:n.939+379A>G
|
|
|
ENST00000509493.1:c.474A>G
|
ENSP00000426757.1:p.Gly158=
|
|
NM_001184741.1:c.954A>G
|
NP_001171670.1:p.Gly318=
|
|
NM_005141.4:c.1131A>G , LRG_558t1:c.1131A>G
|
NP_005132.2:p.Gly377=
|
|
NM_001382759.1:c.999A>G
|
NP_001369688.1:p.Gly333=
|
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NM_001382760.1:c.1131A>G
|
NP_001369689.1:p.Gly377=
|
|
NM_001382761.1:c.1131A>G
|
NP_001369690.1:p.Gly377=
|
|
NM_001382762.1:c.831A>G
|
NP_001369691.1:p.Gly277=
|
|
NM_001382763.1:c.1122A>G
|
NP_001369692.1:p.Gly374=
|
|
NM_001382764.1:c.1080+51A>G
|
NP_001369693.1:n.1080+51A>G
|
|
NM_001382765.1:c.1131A>G
|
NP_001369694.1:p.Gly377=
|
|
NM_005141.5:c.1131A>G
MANE Select
|
NP_005132.2:p.Gly377=
|
|