|
ENST00000261769.10:c.2345T>A
MANE Select
|
ENSP00000261769.4:p.Val782Glu
|
|
|
ENST00000261769.9:c.2345T>A
|
ENSP00000261769.4:p.Val782Glu
|
|
|
ENST00000422392.6:c.2162T>A
|
ENSP00000414946.2:p.Val721Glu
|
|
|
ENST00000562118.1:n.563T>A
|
|
|
|
ENST00000562836.5:n.2416T>A
|
|
|
|
ENST00000566510.5:c.*1011T>A
|
ENSP00000458139.1:n.*1011T>A
|
|
|
ENST00000566612.5:c.*585T>A
|
ENSP00000454782.1:n.*585T>A
|
|
|
ENST00000611625.4:c.2408T>A
|
ENSP00000481063.1:p.Val803Glu
|
|
|
ENST00000612417.4:c.1853+3149T>A
|
ENSP00000478360.1:n.1853+3149T>A
|
|
|
ENST00000621016.4:c.1866-4500T>A
|
ENSP00000480664.1:n.1866-4500T>A
|
|
|
NM_004360.3:c.2345T>A , LRG_301t1:c.2345T>A
|
NP_004351.1:p.Val782Glu
|
|
|
XM_011523488.1:c.1610T>A
|
XP_011521790.1:p.Val537Glu
|
|
|
XM_011523489.1:c.1610T>A
|
XP_011521791.1:p.Val537Glu
|
|
|
NM_001317184.1:c.2162T>A
|
NP_001304113.1:p.Val721Glu
|
|
|
NM_001317185.1:c.797T>A
|
NP_001304114.1:p.Val266Glu
|
|
|
NM_001317186.1:c.380T>A
|
NP_001304115.1:p.Val127Glu
|
|
|
NM_004360.4:c.2345T>A
|
NP_004351.1:p.Val782Glu
|
|
|
NM_004360.5:c.2345T>A
MANE Select
|
NP_004351.1:p.Val782Glu
|
|
|
NM_001317184.2:c.2162T>A
|
NP_001304113.1:p.Val721Glu
|
|
|
NM_001317185.2:c.797T>A
|
NP_001304114.1:p.Val266Glu
|
|
|
NM_001317186.2:c.380T>A
|
NP_001304115.1:p.Val127Glu
|
|
