ENST00000695850.1:n.1471G>T
|
|
|
ENST00000695852.1:n.402G>T
|
|
|
ENST00000695853.1:c.*1354G>T
|
ENSP00000512218.1:n.*1354G>T
|
|
ENST00000423902.7:c.8295G>T
MANE Select
|
ENSP00000392028.1:p.Gln2765His
|
|
ENST00000423902.6:c.8295G>T
|
ENSP00000392028.1:p.Gln2765His
|
|
ENST00000524602.5:c.2148G>T
|
ENSP00000437061.1:p.Gln716His
|
|
ENST00000528280.1:n.341G>T
|
|
|
NM_001316690.1:c.2148G>T
|
NP_001303619.1:p.Gln716His
|
|
NM_017780.3:c.8295G>T
|
NP_060250.2:p.Gln2765His
|
|
XM_011517553.1:c.8385G>T
|
XP_011515855.1:p.Gln2795His
|
|
XM_011517554.1:c.8385G>T
|
XP_011515856.1:p.Gln2795His
|
|
XM_011517555.1:c.8382G>T
|
XP_011515857.1:p.Gln2794His
|
|
XM_011517556.1:c.8163G>T
|
XP_011515858.1:p.Gln2721His
|
|
XM_011517557.1:c.6372G>T
|
XP_011515859.1:p.Gln2124His
|
|
XM_011517558.1:c.5922G>T
|
XP_011515860.1:p.Gln1974His
|
|
XM_011517559.1:c.5130G>T
|
XP_011515861.1:p.Gln1710His
|
|
XM_011517553.2:c.8385G>T
|
XP_011515855.1:p.Gln2795His
|
|
XM_011517554.3:c.8385G>T
|
XP_011515856.1:p.Gln2795His
|
|
XM_011517555.2:c.8382G>T
|
XP_011515857.1:p.Gln2794His
|
|
XM_017013612.1:c.8385G>T
|
XP_016869101.1:p.Gln2795His
|
|
XM_017013613.1:c.8292G>T
|
XP_016869102.1:p.Gln2764His
|
|
NM_017780.4:c.8295G>T
MANE Select
|
NP_060250.2:p.Gln2765His
|
|