ENST00000263038.9:c.819A>C
MANE Select
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ENSP00000263038.4:p.Gly273=
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ENST00000263038.8:c.819A>C
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ENSP00000263038.4:p.Gly273=
|
|
ENST00000396913.6:c.519A>C
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ENSP00000380121.2:p.Gly173=
|
|
ENST00000396920.7:c.768A>C
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ENSP00000380126.3:p.Gly256=
|
|
ENST00000453759.6:c.519A>C
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ENSP00000412525.2:p.Gly173=
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|
NM_001037537.1:c.519A>C
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NP_001032626.1:p.Gly173=
|
|
NM_006214.3:c.819A>C
|
NP_006205.1:p.Gly273=
|
|
XM_005252469.2:c.600A>C
|
XP_005252526.1:p.Gly200=
|
|
NM_001323080.1:c.519A>C
|
NP_001310009.1:p.Gly173=
|
|
NM_001323082.1:c.825A>C
|
NP_001310011.1:p.Gly275=
|
|
NM_001323083.1:c.555A>C
|
NP_001310012.1:p.Gly185=
|
|
NM_001323084.1:c.525A>C
|
NP_001310013.1:p.Gly175=
|
|
NM_006214.4:c.819A>C
MANE Select
|
NP_006205.1:p.Gly273=
|
|
NM_001037537.2:c.519A>C
|
NP_001032626.1:p.Gly173=
|
|
NM_001323080.2:c.519A>C
|
NP_001310009.1:p.Gly173=
|
|
NM_001323082.2:c.825A>C
|
NP_001310011.1:p.Gly275=
|
|
NM_001323083.2:c.555A>C
|
NP_001310012.1:p.Gly185=
|
|
NM_001323084.2:c.525A>C
|
NP_001310013.1:p.Gly175=
|
|