ENST00000695853.1:c.6186G>C
|
ENSP00000512218.1:p.Arg2062=
|
|
ENST00000423902.7:c.6186G>C
MANE Select
|
ENSP00000392028.1:p.Arg2062=
|
|
ENST00000423902.6:c.6186G>C
|
ENSP00000392028.1:p.Arg2062=
|
|
ENST00000524602.5:c.1717-9318G>C
|
ENSP00000437061.1:n.1717-9318G>C
|
|
NM_001316690.1:c.1717-9318G>C
|
NP_001303619.1:n.1717-9318G>C
|
|
NM_017780.3:c.6186G>C
|
NP_060250.2:p.Arg2062=
|
|
XM_011517553.1:c.6276G>C
|
XP_011515855.1:p.Arg2092=
|
|
XM_011517554.1:c.6276G>C
|
XP_011515856.1:p.Arg2092=
|
|
XM_011517555.1:c.6276G>C
|
XP_011515857.1:p.Arg2092=
|
|
XM_011517556.1:c.6276G>C
|
XP_011515858.1:p.Arg2092=
|
|
XM_011517557.1:c.4263G>C
|
XP_011515859.1:p.Arg1421=
|
|
XM_011517558.1:c.3813G>C
|
XP_011515860.1:p.Arg1271=
|
|
XM_011517559.1:c.3021G>C
|
XP_011515861.1:p.Arg1007=
|
|
XM_011517553.2:c.6276G>C
|
XP_011515855.1:p.Arg2092=
|
|
XM_011517554.3:c.6276G>C
|
XP_011515856.1:p.Arg2092=
|
|
XM_011517555.2:c.6276G>C
|
XP_011515857.1:p.Arg2092=
|
|
XM_017013612.1:c.6276G>C
|
XP_016869101.1:p.Arg2092=
|
|
XM_017013613.1:c.6186G>C
|
XP_016869102.1:p.Arg2062=
|
|
NM_017780.4:c.6186G>C
MANE Select
|
NP_060250.2:p.Arg2062=
|
|