ENST00000695850.1:n.1430G>C
|
|
|
ENST00000695852.1:n.361G>C
|
|
|
ENST00000695853.1:c.*1313G>C
|
ENSP00000512218.1:n.*1313G>C
|
|
ENST00000423902.7:c.8254G>C
MANE Select
|
ENSP00000392028.1:p.Gly2752Arg
|
|
ENST00000423902.6:c.8254G>C
|
ENSP00000392028.1:p.Gly2752Arg
|
|
ENST00000524602.5:c.2107G>C
|
ENSP00000437061.1:p.Gly703Arg
|
|
ENST00000528280.1:n.300G>C
|
|
|
NM_001316690.1:c.2107G>C
|
NP_001303619.1:p.Gly703Arg
|
|
NM_017780.3:c.8254G>C
|
NP_060250.2:p.Gly2752Arg
|
|
XM_011517553.1:c.8344G>C
|
XP_011515855.1:p.Gly2782Arg
|
|
XM_011517554.1:c.8344G>C
|
XP_011515856.1:p.Gly2782Arg
|
|
XM_011517555.1:c.8341G>C
|
XP_011515857.1:p.Gly2781Arg
|
|
XM_011517556.1:c.8122G>C
|
XP_011515858.1:p.Gly2708Arg
|
|
XM_011517557.1:c.6331G>C
|
XP_011515859.1:p.Gly2111Arg
|
|
XM_011517558.1:c.5881G>C
|
XP_011515860.1:p.Gly1961Arg
|
|
XM_011517559.1:c.5089G>C
|
XP_011515861.1:p.Gly1697Arg
|
|
XM_011517553.2:c.8344G>C
|
XP_011515855.1:p.Gly2782Arg
|
|
XM_011517554.3:c.8344G>C
|
XP_011515856.1:p.Gly2782Arg
|
|
XM_011517555.2:c.8341G>C
|
XP_011515857.1:p.Gly2781Arg
|
|
XM_017013612.1:c.8344G>C
|
XP_016869101.1:p.Gly2782Arg
|
|
XM_017013613.1:c.8251G>C
|
XP_016869102.1:p.Gly2751Arg
|
|
NM_017780.4:c.8254G>C
MANE Select
|
NP_060250.2:p.Gly2752Arg
|
|