ENST00000261769.10:c.2639A=
MANE Select
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ENSP00000261769.4:p.Glu880=
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ENST00000261769.9:c.2639A=
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ENSP00000261769.4:p.Glu880=
|
|
ENST00000422392.6:c.2456A=
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ENSP00000414946.2:p.Glu819=
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ENST00000562118.1:n.857A=
|
|
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ENST00000562836.5:n.2710A=
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|
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ENST00000566510.5:c.*1305A=
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ENSP00000458139.1:n.*1305A=
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|
ENST00000566612.5:c.*879A=
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ENSP00000454782.1:n.*879A=
|
|
ENST00000611625.4:c.2702A=
|
ENSP00000481063.1:p.Glu901=
|
|
ENST00000612417.4:c.1854-702A=
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ENSP00000478360.1:n.1854-702A=
|
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ENST00000621016.4:c.1866-714A=
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ENSP00000480664.1:n.1866-714A=
|
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NM_004360.3:c.2639A= , LRG_301t1:c.2639A=
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NP_004351.1:p.Glu880=
|
|
XM_011523488.1:c.1904A=
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XP_011521790.1:p.Glu635=
|
|
XM_011523489.1:c.1904A=
|
XP_011521791.1:p.Glu635=
|
|
NM_001317184.1:c.2456A=
|
NP_001304113.1:p.Glu819=
|
|
NM_001317185.1:c.1091A=
|
NP_001304114.1:p.Glu364=
|
|
NM_001317186.1:c.674A=
|
NP_001304115.1:p.Glu225=
|
|
NM_004360.4:c.2639A=
|
NP_004351.1:p.Glu880=
|
|
NM_004360.5:c.2639A=
MANE Select
|
NP_004351.1:p.Glu880=
|
|
NM_001317184.2:c.2456A=
|
NP_001304113.1:p.Glu819=
|
|
NM_001317185.2:c.1091A=
|
NP_001304114.1:p.Glu364=
|
|
NM_001317186.2:c.674A=
|
NP_001304115.1:p.Glu225=
|
|