ENST00000695850.1:n.1423G>T
|
|
|
ENST00000695852.1:n.354G>T
|
|
|
ENST00000695853.1:c.*1306G>T
|
ENSP00000512218.1:n.*1306G>T
|
|
ENST00000423902.7:c.8247G>T
MANE Select
|
ENSP00000392028.1:p.Leu2749=
|
|
ENST00000423902.6:c.8247G>T
|
ENSP00000392028.1:p.Leu2749=
|
|
ENST00000524602.5:c.2100G>T
|
ENSP00000437061.1:p.Leu700=
|
|
ENST00000528280.1:n.293G>T
|
|
|
NM_001316690.1:c.2100G>T
|
NP_001303619.1:p.Leu700=
|
|
NM_017780.3:c.8247G>T
|
NP_060250.2:p.Leu2749=
|
|
XM_011517553.1:c.8337G>T
|
XP_011515855.1:p.Leu2779=
|
|
XM_011517554.1:c.8337G>T
|
XP_011515856.1:p.Leu2779=
|
|
XM_011517555.1:c.8334G>T
|
XP_011515857.1:p.Leu2778=
|
|
XM_011517556.1:c.8115G>T
|
XP_011515858.1:p.Leu2705=
|
|
XM_011517557.1:c.6324G>T
|
XP_011515859.1:p.Leu2108=
|
|
XM_011517558.1:c.5874G>T
|
XP_011515860.1:p.Leu1958=
|
|
XM_011517559.1:c.5082G>T
|
XP_011515861.1:p.Leu1694=
|
|
XM_011517553.2:c.8337G>T
|
XP_011515855.1:p.Leu2779=
|
|
XM_011517554.3:c.8337G>T
|
XP_011515856.1:p.Leu2779=
|
|
XM_011517555.2:c.8334G>T
|
XP_011515857.1:p.Leu2778=
|
|
XM_017013612.1:c.8337G>T
|
XP_016869101.1:p.Leu2779=
|
|
XM_017013613.1:c.8244G>T
|
XP_016869102.1:p.Leu2748=
|
|
NM_017780.4:c.8247G>T
MANE Select
|
NP_060250.2:p.Leu2749=
|
|