ENST00000263967.4:c.1749G=
MANE Select
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ENSP00000263967.3:p.Met583=
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ENST00000462255.2:n.211G=
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|
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ENST00000643187.1:c.1749G=
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ENSP00000493507.1:p.Met583=
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|
ENST00000674534.1:n.2657G=
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|
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ENST00000674622.1:c.170G=
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ENSP00000502417.1:p.Cys57=
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|
ENST00000675467.1:n.4556G=
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|
|
ENST00000675786.1:c.*316G=
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ENSP00000502323.1:n.*316G=
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|
ENST00000263967.3:c.1749G=
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ENSP00000263967.3:p.Met583=
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ENST00000462255.1:n.23G=
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|
|
NM_006218.2:c.1749G= , LRG_310t1:c.1749G=
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NP_006209.2:p.Met583=
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|
XM_006713658.2:c.1749G=
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XP_006713721.1:p.Met583=
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|
XM_011512894.1:c.1749G=
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XP_011511196.1:p.Met583=
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|
NM_006218.3:c.1749G=
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NP_006209.2:p.Met583=
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|
XM_006713658.4:c.1749G=
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XP_006713721.1:p.Met583=
|
|
XM_011512894.2:c.1749G=
|
XP_011511196.1:p.Met583=
|
|
NM_006218.4:c.1749G=
MANE Select
|
NP_006209.2:p.Met583=
|
|