|
ENST00000370695.8:c.121G>C
|
ENSP00000359729.4:p.Gly41Arg
|
|
|
ENST00000370701.6:c.-36G>C
|
ENSP00000359735.1:n.-36G>C
|
|
|
ENST00000630721.3:c.-36G>C
MANE Select
|
ENSP00000487486.2:n.-36G>C
|
|
|
ENST00000636092.1:c.-36G>C
|
ENSP00000490406.1:n.-36G>C
|
|
|
ENST00000636347.1:c.-35-1G>C
|
ENSP00000490648.1:n.-35-1G>C
|
|
|
ENST00000637195.1:c.-35-1G>C
|
ENSP00000490330.1:n.-35-1G>C
|
|
|
ENST00000637234.1:c.-36G>C
|
ENSP00000490527.1:n.-36G>C
|
|
|
ENST00000637581.1:c.-36G>C
|
ENSP00000490731.1:n.-36G>C
|
|
|
ENST00000678163.1:c.121G>C
|
ENSP00000502845.1:p.Gly41Arg
|
|
|
ENST00000370695.6:c.121G>C
|
ENSP00000359729.4:p.Gly41Arg
|
|
|
ENST00000370698.7:c.121G>C
|
ENSP00000359732.3:p.Gly41Arg
|
|
|
ENST00000370701.5:c.-36G>C
|
ENSP00000359735.1:n.-36G>C
|
|
|
ENST00000627534.2:c.-36G>C
|
ENSP00000486743.1:n.-36G>C
|
|
|
NM_001042537.1:c.121G>C
|
NP_001036002.1:p.Gly41Arg
|
|
|
NM_001177651.1:c.-36G>C
|
NP_001171122.1:n.-36G>C
|
|
|
NM_006359.2:c.121G>C
|
NP_006350.1:p.Gly41Arg
|
|
|
XM_006724726.2:c.-36G>C
|
XP_006724789.1:n.-36G>C
|
|
|
XM_011531243.1:c.-36G>C
|
XP_011529545.1:n.-36G>C
|
|
|
NM_001330652.1:c.-36G>C
|
NP_001317581.1:n.-36G>C
|
|
|
XM_006724726.3:c.-36G>C
|
XP_006724789.1:n.-36G>C
|
|
|
XM_017029223.2:c.-36G>C
|
XP_016884712.1:n.-36G>C
|
|
|
XM_017029224.1:c.-36G>C
|
XP_016884713.1:n.-36G>C
|
|
|
XM_017029225.1:c.-36G>C
|
XP_016884714.1:n.-36G>C
|
|
|
NM_001177651.2:c.-36G>C
|
NP_001171122.1:n.-36G>C
|
|
|
NM_001330652.2:c.-36G>C
|
NP_001317581.1:n.-36G>C
|
|
|
NM_006359.3:c.121G>C
|
NP_006350.1:p.Gly41Arg
|
|
|
NM_001042537.2:c.121G>C
|
NP_001036002.1:p.Gly41Arg
|
|
|
NM_001379110.1:c.-36G>C
MANE Select
|
NP_001366039.1:n.-36G>C
|
|
|
NM_001400909.1:c.-35-1G>C
|
NP_001387838.1:n.-35-1G>C
|
|
|
NM_001400910.1:c.-36G>C
|
NP_001387839.1:n.-36G>C
|
|
|
NM_001400911.1:c.-36G>C
|
NP_001387840.1:n.-36G>C
|
|
|
NM_001400912.1:c.-36G>C
|
NP_001387841.1:n.-36G>C
|
|
|
NM_001400913.1:c.-36G>C
|
NP_001387842.1:n.-36G>C
|
|
