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ENST00000261769.10:c.2567A>C
MANE Select
|
ENSP00000261769.4:p.Asp856Ala
|
|
|
ENST00000261769.9:c.2567A>C
|
ENSP00000261769.4:p.Asp856Ala
|
|
|
ENST00000422392.6:c.2384A>C
|
ENSP00000414946.2:p.Asp795Ala
|
|
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ENST00000562118.1:n.785A>C
|
|
|
|
ENST00000562836.5:n.2638A>C
|
|
|
|
ENST00000566510.5:c.*1233A>C
|
ENSP00000458139.1:n.*1233A>C
|
|
|
ENST00000566612.5:c.*807A>C
|
ENSP00000454782.1:n.*807A>C
|
|
|
ENST00000611625.4:c.2630A>C
|
ENSP00000481063.1:p.Asp877Ala
|
|
|
ENST00000612417.4:c.1854-774A>C
|
ENSP00000478360.1:n.1854-774A>C
|
|
|
ENST00000621016.4:c.1866-786A>C
|
ENSP00000480664.1:n.1866-786A>C
|
|
|
NM_004360.3:c.2567A>C , LRG_301t1:c.2567A>C
|
NP_004351.1:p.Asp856Ala
|
|
|
XM_011523488.1:c.1832A>C
|
XP_011521790.1:p.Asp611Ala
|
|
|
XM_011523489.1:c.1832A>C
|
XP_011521791.1:p.Asp611Ala
|
|
|
NM_001317184.1:c.2384A>C
|
NP_001304113.1:p.Asp795Ala
|
|
|
NM_001317185.1:c.1019A>C
|
NP_001304114.1:p.Asp340Ala
|
|
|
NM_001317186.1:c.602A>C
|
NP_001304115.1:p.Asp201Ala
|
|
|
NM_004360.4:c.2567A>C
|
NP_004351.1:p.Asp856Ala
|
|
|
NM_004360.5:c.2567A>C
MANE Select
|
NP_004351.1:p.Asp856Ala
|
|
|
NM_001317184.2:c.2384A>C
|
NP_001304113.1:p.Asp795Ala
|
|
|
NM_001317185.2:c.1019A>C
|
NP_001304114.1:p.Asp340Ala
|
|
|
NM_001317186.2:c.602A>C
|
NP_001304115.1:p.Asp201Ala
|
|
