ENST00000695850.1:n.1441G>C
|
|
|
ENST00000695852.1:n.372G>C
|
|
|
ENST00000695853.1:c.*1324G>C
|
ENSP00000512218.1:n.*1324G>C
|
|
ENST00000423902.7:c.8265G>C
MANE Select
|
ENSP00000392028.1:p.Leu2755=
|
|
ENST00000423902.6:c.8265G>C
|
ENSP00000392028.1:p.Leu2755=
|
|
ENST00000524602.5:c.2118G>C
|
ENSP00000437061.1:p.Leu706=
|
|
ENST00000528280.1:n.311G>C
|
|
|
NM_001316690.1:c.2118G>C
|
NP_001303619.1:p.Leu706=
|
|
NM_017780.3:c.8265G>C
|
NP_060250.2:p.Leu2755=
|
|
XM_011517553.1:c.8355G>C
|
XP_011515855.1:p.Leu2785=
|
|
XM_011517554.1:c.8355G>C
|
XP_011515856.1:p.Leu2785=
|
|
XM_011517555.1:c.8352G>C
|
XP_011515857.1:p.Leu2784=
|
|
XM_011517556.1:c.8133G>C
|
XP_011515858.1:p.Leu2711=
|
|
XM_011517557.1:c.6342G>C
|
XP_011515859.1:p.Leu2114=
|
|
XM_011517558.1:c.5892G>C
|
XP_011515860.1:p.Leu1964=
|
|
XM_011517559.1:c.5100G>C
|
XP_011515861.1:p.Leu1700=
|
|
XM_011517553.2:c.8355G>C
|
XP_011515855.1:p.Leu2785=
|
|
XM_011517554.3:c.8355G>C
|
XP_011515856.1:p.Leu2785=
|
|
XM_011517555.2:c.8352G>C
|
XP_011515857.1:p.Leu2784=
|
|
XM_017013612.1:c.8355G>C
|
XP_016869101.1:p.Leu2785=
|
|
XM_017013613.1:c.8262G>C
|
XP_016869102.1:p.Leu2754=
|
|
NM_017780.4:c.8265G>C
MANE Select
|
NP_060250.2:p.Leu2755=
|
|