|
ENST00000261769.10:c.2341G>C
MANE Select
|
ENSP00000261769.4:p.Glu781Gln
|
|
|
ENST00000261769.9:c.2341G>C
|
ENSP00000261769.4:p.Glu781Gln
|
|
|
ENST00000422392.6:c.2158G>C
|
ENSP00000414946.2:p.Glu720Gln
|
|
|
ENST00000562118.1:n.559G>C
|
|
|
|
ENST00000562836.5:n.2412G>C
|
|
|
|
ENST00000566510.5:c.*1007G>C
|
ENSP00000458139.1:n.*1007G>C
|
|
|
ENST00000566612.5:c.*581G>C
|
ENSP00000454782.1:n.*581G>C
|
|
|
ENST00000611625.4:c.2404G>C
|
ENSP00000481063.1:p.Glu802Gln
|
|
|
ENST00000612417.4:c.1853+3145G>C
|
ENSP00000478360.1:n.1853+3145G>C
|
|
|
ENST00000621016.4:c.1866-4504G>C
|
ENSP00000480664.1:n.1866-4504G>C
|
|
|
NM_004360.3:c.2341G>C , LRG_301t1:c.2341G>C
|
NP_004351.1:p.Glu781Gln
|
|
|
XM_011523488.1:c.1606G>C
|
XP_011521790.1:p.Glu536Gln
|
|
|
XM_011523489.1:c.1606G>C
|
XP_011521791.1:p.Glu536Gln
|
|
|
NM_001317184.1:c.2158G>C
|
NP_001304113.1:p.Glu720Gln
|
|
|
NM_001317185.1:c.793G>C
|
NP_001304114.1:p.Glu265Gln
|
|
|
NM_001317186.1:c.376G>C
|
NP_001304115.1:p.Glu126Gln
|
|
|
NM_004360.4:c.2341G>C
|
NP_004351.1:p.Glu781Gln
|
|
|
NM_004360.5:c.2341G>C
MANE Select
|
NP_004351.1:p.Glu781Gln
|
|
|
NM_001317184.2:c.2158G>C
|
NP_001304113.1:p.Glu720Gln
|
|
|
NM_001317185.2:c.793G>C
|
NP_001304114.1:p.Glu265Gln
|
|
|
NM_001317186.2:c.376G>C
|
NP_001304115.1:p.Glu126Gln
|
|
