ENST00000695850.1:n.1451C>T
|
|
|
ENST00000695852.1:n.382C>T
|
|
|
ENST00000695853.1:c.*1334C>T
|
ENSP00000512218.1:n.*1334C>T
|
|
ENST00000423902.7:c.8275C>T
MANE Select
|
ENSP00000392028.1:p.Gln2759Ter
|
|
ENST00000423902.6:c.8275C>T
|
ENSP00000392028.1:p.Gln2759Ter
|
|
ENST00000524602.5:c.2128C>T
|
ENSP00000437061.1:p.Gln710Ter
|
|
ENST00000528280.1:n.321C>T
|
|
|
NM_001316690.1:c.2128C>T
|
NP_001303619.1:p.Gln710Ter
|
|
NM_017780.3:c.8275C>T
|
NP_060250.2:p.Gln2759Ter
|
|
XM_011517553.1:c.8365C>T
|
XP_011515855.1:p.Gln2789Ter
|
|
XM_011517554.1:c.8365C>T
|
XP_011515856.1:p.Gln2789Ter
|
|
XM_011517555.1:c.8362C>T
|
XP_011515857.1:p.Gln2788Ter
|
|
XM_011517556.1:c.8143C>T
|
XP_011515858.1:p.Gln2715Ter
|
|
XM_011517557.1:c.6352C>T
|
XP_011515859.1:p.Gln2118Ter
|
|
XM_011517558.1:c.5902C>T
|
XP_011515860.1:p.Gln1968Ter
|
|
XM_011517559.1:c.5110C>T
|
XP_011515861.1:p.Gln1704Ter
|
|
XM_011517553.2:c.8365C>T
|
XP_011515855.1:p.Gln2789Ter
|
|
XM_011517554.3:c.8365C>T
|
XP_011515856.1:p.Gln2789Ter
|
|
XM_011517555.2:c.8362C>T
|
XP_011515857.1:p.Gln2788Ter
|
|
XM_017013612.1:c.8365C>T
|
XP_016869101.1:p.Gln2789Ter
|
|
XM_017013613.1:c.8272C>T
|
XP_016869102.1:p.Gln2758Ter
|
|
NM_017780.4:c.8275C>T
MANE Select
|
NP_060250.2:p.Gln2759Ter
|
|