ENST00000695850.1:n.1477C>A
|
|
|
ENST00000695852.1:n.408C>A
|
|
|
ENST00000695853.1:c.*1360C>A
|
ENSP00000512218.1:n.*1360C>A
|
|
ENST00000423902.7:c.8301C>A
MANE Select
|
ENSP00000392028.1:p.Leu2767=
|
|
ENST00000423902.6:c.8301C>A
|
ENSP00000392028.1:p.Leu2767=
|
|
ENST00000524602.5:c.2154C>A
|
ENSP00000437061.1:p.Leu718=
|
|
ENST00000528280.1:n.347C>A
|
|
|
NM_001316690.1:c.2154C>A
|
NP_001303619.1:p.Leu718=
|
|
NM_017780.3:c.8301C>A
|
NP_060250.2:p.Leu2767=
|
|
XM_011517553.1:c.8391C>A
|
XP_011515855.1:p.Leu2797=
|
|
XM_011517554.1:c.8391C>A
|
XP_011515856.1:p.Leu2797=
|
|
XM_011517555.1:c.8388C>A
|
XP_011515857.1:p.Leu2796=
|
|
XM_011517556.1:c.8169C>A
|
XP_011515858.1:p.Leu2723=
|
|
XM_011517557.1:c.6378C>A
|
XP_011515859.1:p.Leu2126=
|
|
XM_011517558.1:c.5928C>A
|
XP_011515860.1:p.Leu1976=
|
|
XM_011517559.1:c.5136C>A
|
XP_011515861.1:p.Leu1712=
|
|
XM_011517553.2:c.8391C>A
|
XP_011515855.1:p.Leu2797=
|
|
XM_011517554.3:c.8391C>A
|
XP_011515856.1:p.Leu2797=
|
|
XM_011517555.2:c.8388C>A
|
XP_011515857.1:p.Leu2796=
|
|
XM_017013612.1:c.8391C>A
|
XP_016869101.1:p.Leu2797=
|
|
XM_017013613.1:c.8298C>A
|
XP_016869102.1:p.Leu2766=
|
|
NM_017780.4:c.8301C>A
MANE Select
|
NP_060250.2:p.Leu2767=
|
|