ENST00000695850.1:n.1458T>A
|
|
|
ENST00000695852.1:n.389T>A
|
|
|
ENST00000695853.1:c.*1341T>A
|
ENSP00000512218.1:n.*1341T>A
|
|
ENST00000423902.7:c.8282T>A
MANE Select
|
ENSP00000392028.1:p.Leu2761His
|
|
ENST00000423902.6:c.8282T>A
|
ENSP00000392028.1:p.Leu2761His
|
|
ENST00000524602.5:c.2135T>A
|
ENSP00000437061.1:p.Leu712His
|
|
ENST00000528280.1:n.328T>A
|
|
|
NM_001316690.1:c.2135T>A
|
NP_001303619.1:p.Leu712His
|
|
NM_017780.3:c.8282T>A
|
NP_060250.2:p.Leu2761His
|
|
XM_011517553.1:c.8372T>A
|
XP_011515855.1:p.Leu2791His
|
|
XM_011517554.1:c.8372T>A
|
XP_011515856.1:p.Leu2791His
|
|
XM_011517555.1:c.8369T>A
|
XP_011515857.1:p.Leu2790His
|
|
XM_011517556.1:c.8150T>A
|
XP_011515858.1:p.Leu2717His
|
|
XM_011517557.1:c.6359T>A
|
XP_011515859.1:p.Leu2120His
|
|
XM_011517558.1:c.5909T>A
|
XP_011515860.1:p.Leu1970His
|
|
XM_011517559.1:c.5117T>A
|
XP_011515861.1:p.Leu1706His
|
|
XM_011517553.2:c.8372T>A
|
XP_011515855.1:p.Leu2791His
|
|
XM_011517554.3:c.8372T>A
|
XP_011515856.1:p.Leu2791His
|
|
XM_011517555.2:c.8369T>A
|
XP_011515857.1:p.Leu2790His
|
|
XM_017013612.1:c.8372T>A
|
XP_016869101.1:p.Leu2791His
|
|
XM_017013613.1:c.8279T>A
|
XP_016869102.1:p.Leu2760His
|
|
NM_017780.4:c.8282T>A
MANE Select
|
NP_060250.2:p.Leu2761His
|
|