ENST00000211998.10:c.1051C=
MANE Select
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ENSP00000211998.5:p.Gln351=
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ENST00000211998.8:c.1051C=
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ENSP00000211998.4:p.Gln351=
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|
ENST00000372755.7:c.1051C=
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ENSP00000361841.3:p.Gln351=
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|
ENST00000436396.1:c.67C=
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ENSP00000415489.1:p.Gln23=
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|
ENST00000478896.2:n.332-11830C=
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|
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ENST00000623461.3:n.3854C=
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|
|
ENST00000624354.3:c.*806C=
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ENSP00000485551.1:n.*806C=
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|
NM_003373.3:c.1051C=
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NP_003364.1:p.Gln351=
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|
NM_014000.2:c.1051C= , LRG_383t1:c.1051C=
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NP_054706.1:p.Gln351=
|
|
XM_005270142.1:c.1054C=
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XP_005270199.1:p.Gln352=
|
|
XM_005270143.1:c.1054C=
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XP_005270200.1:p.Gln352=
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|
XR_001747501.1:n.89+708G=
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|
|
NM_003373.4:c.1051C=
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NP_003364.1:p.Gln351=
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|
NM_014000.3:c.1051C=
MANE Select
|
NP_054706.1:p.Gln351=
|
|