ENST00000695850.1:n.1450T>G
|
|
|
ENST00000695852.1:n.381T>G
|
|
|
ENST00000695853.1:c.*1333T>G
|
ENSP00000512218.1:n.*1333T>G
|
|
ENST00000423902.7:c.8274T>G
MANE Select
|
ENSP00000392028.1:p.Leu2758=
|
|
ENST00000423902.6:c.8274T>G
|
ENSP00000392028.1:p.Leu2758=
|
|
ENST00000524602.5:c.2127T>G
|
ENSP00000437061.1:p.Leu709=
|
|
ENST00000528280.1:n.320T>G
|
|
|
NM_001316690.1:c.2127T>G
|
NP_001303619.1:p.Leu709=
|
|
NM_017780.3:c.8274T>G
|
NP_060250.2:p.Leu2758=
|
|
XM_011517553.1:c.8364T>G
|
XP_011515855.1:p.Leu2788=
|
|
XM_011517554.1:c.8364T>G
|
XP_011515856.1:p.Leu2788=
|
|
XM_011517555.1:c.8361T>G
|
XP_011515857.1:p.Leu2787=
|
|
XM_011517556.1:c.8142T>G
|
XP_011515858.1:p.Leu2714=
|
|
XM_011517557.1:c.6351T>G
|
XP_011515859.1:p.Leu2117=
|
|
XM_011517558.1:c.5901T>G
|
XP_011515860.1:p.Leu1967=
|
|
XM_011517559.1:c.5109T>G
|
XP_011515861.1:p.Leu1703=
|
|
XM_011517553.2:c.8364T>G
|
XP_011515855.1:p.Leu2788=
|
|
XM_011517554.3:c.8364T>G
|
XP_011515856.1:p.Leu2788=
|
|
XM_011517555.2:c.8361T>G
|
XP_011515857.1:p.Leu2787=
|
|
XM_017013612.1:c.8364T>G
|
XP_016869101.1:p.Leu2788=
|
|
XM_017013613.1:c.8271T>G
|
XP_016869102.1:p.Leu2757=
|
|
NM_017780.4:c.8274T>G
MANE Select
|
NP_060250.2:p.Leu2758=
|
|