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ENST00000261769.10:c.2579A>C
MANE Select
|
ENSP00000261769.4:p.Asp860Ala
|
|
|
ENST00000261769.9:c.2579A>C
|
ENSP00000261769.4:p.Asp860Ala
|
|
|
ENST00000422392.6:c.2396A>C
|
ENSP00000414946.2:p.Asp799Ala
|
|
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ENST00000562118.1:n.797A>C
|
|
|
|
ENST00000562836.5:n.2650A>C
|
|
|
|
ENST00000566510.5:c.*1245A>C
|
ENSP00000458139.1:n.*1245A>C
|
|
|
ENST00000566612.5:c.*819A>C
|
ENSP00000454782.1:n.*819A>C
|
|
|
ENST00000611625.4:c.2642A>C
|
ENSP00000481063.1:p.Asp881Ala
|
|
|
ENST00000612417.4:c.1854-762A>C
|
ENSP00000478360.1:n.1854-762A>C
|
|
|
ENST00000621016.4:c.1866-774A>C
|
ENSP00000480664.1:n.1866-774A>C
|
|
|
NM_004360.3:c.2579A>C , LRG_301t1:c.2579A>C
|
NP_004351.1:p.Asp860Ala
|
|
|
XM_011523488.1:c.1844A>C
|
XP_011521790.1:p.Asp615Ala
|
|
|
XM_011523489.1:c.1844A>C
|
XP_011521791.1:p.Asp615Ala
|
|
|
NM_001317184.1:c.2396A>C
|
NP_001304113.1:p.Asp799Ala
|
|
|
NM_001317185.1:c.1031A>C
|
NP_001304114.1:p.Asp344Ala
|
|
|
NM_001317186.1:c.614A>C
|
NP_001304115.1:p.Asp205Ala
|
|
|
NM_004360.4:c.2579A>C
|
NP_004351.1:p.Asp860Ala
|
|
|
NM_004360.5:c.2579A>C
MANE Select
|
NP_004351.1:p.Asp860Ala
|
|
|
NM_001317184.2:c.2396A>C
|
NP_001304113.1:p.Asp799Ala
|
|
|
NM_001317185.2:c.1031A>C
|
NP_001304114.1:p.Asp344Ala
|
|
|
NM_001317186.2:c.614A>C
|
NP_001304115.1:p.Asp205Ala
|
|
