ENST00000695850.1:n.1334A>G
|
|
|
ENST00000695852.1:n.265A>G
|
|
|
ENST00000695853.1:c.*1217A>G
|
ENSP00000512218.1:n.*1217A>G
|
|
ENST00000423902.7:c.8158A>G
MANE Select
|
ENSP00000392028.1:p.Arg2720Gly
|
|
ENST00000423902.6:c.8158A>G
|
ENSP00000392028.1:p.Arg2720Gly
|
|
ENST00000524602.5:c.2011A>G
|
ENSP00000437061.1:p.Arg671Gly
|
|
ENST00000528280.1:n.204A>G
|
|
|
ENST00000532149.1:n.580A>G
|
|
|
ENST00000618450.1:n.4194A>G
|
|
|
NM_001316690.1:c.2011A>G
|
NP_001303619.1:p.Arg671Gly
|
|
NM_017780.3:c.8158A>G
|
NP_060250.2:p.Arg2720Gly
|
|
XM_011517553.1:c.8248A>G
|
XP_011515855.1:p.Arg2750Gly
|
|
XM_011517554.1:c.8248A>G
|
XP_011515856.1:p.Arg2750Gly
|
|
XM_011517555.1:c.8245A>G
|
XP_011515857.1:p.Arg2749Gly
|
|
XM_011517556.1:c.8026A>G
|
XP_011515858.1:p.Arg2676Gly
|
|
XM_011517557.1:c.6235A>G
|
XP_011515859.1:p.Arg2079Gly
|
|
XM_011517558.1:c.5785A>G
|
XP_011515860.1:p.Arg1929Gly
|
|
XM_011517559.1:c.4993A>G
|
XP_011515861.1:p.Arg1665Gly
|
|
XM_011517553.2:c.8248A>G
|
XP_011515855.1:p.Arg2750Gly
|
|
XM_011517554.3:c.8248A>G
|
XP_011515856.1:p.Arg2750Gly
|
|
XM_011517555.2:c.8245A>G
|
XP_011515857.1:p.Arg2749Gly
|
|
XM_017013612.1:c.8248A>G
|
XP_016869101.1:p.Arg2750Gly
|
|
XM_017013613.1:c.8155A>G
|
XP_016869102.1:p.Arg2719Gly
|
|
NM_017780.4:c.8158A>G
MANE Select
|
NP_060250.2:p.Arg2720Gly
|
|