ENST00000695850.1:n.1679G>T
|
|
|
ENST00000695852.1:n.610G>T
|
|
|
ENST00000695853.1:c.*1562G>T
|
ENSP00000512218.1:n.*1562G>T
|
|
ENST00000423902.7:c.8503G>T
MANE Select
|
ENSP00000392028.1:p.Glu2835Ter
|
|
ENST00000423902.6:c.8503G>T
|
ENSP00000392028.1:p.Glu2835Ter
|
|
ENST00000524602.5:c.2356G>T
|
ENSP00000437061.1:p.Glu786Ter
|
|
ENST00000528280.1:n.549G>T
|
|
|
NM_001316690.1:c.2356G>T
|
NP_001303619.1:p.Glu786Ter
|
|
NM_017780.3:c.8503G>T
|
NP_060250.2:p.Glu2835Ter
|
|
XM_011517553.1:c.8593G>T
|
XP_011515855.1:p.Glu2865Ter
|
|
XM_011517554.1:c.8593G>T
|
XP_011515856.1:p.Glu2865Ter
|
|
XM_011517555.1:c.8590G>T
|
XP_011515857.1:p.Glu2864Ter
|
|
XM_011517556.1:c.8371G>T
|
XP_011515858.1:p.Glu2791Ter
|
|
XM_011517557.1:c.6580G>T
|
XP_011515859.1:p.Glu2194Ter
|
|
XM_011517558.1:c.6130G>T
|
XP_011515860.1:p.Glu2044Ter
|
|
XM_011517559.1:c.5338G>T
|
XP_011515861.1:p.Glu1780Ter
|
|
XM_011517553.2:c.8593G>T
|
XP_011515855.1:p.Glu2865Ter
|
|
XM_011517554.3:c.8593G>T
|
XP_011515856.1:p.Glu2865Ter
|
|
XM_011517555.2:c.8590G>T
|
XP_011515857.1:p.Glu2864Ter
|
|
XM_017013612.1:c.8593G>T
|
XP_016869101.1:p.Glu2865Ter
|
|
XM_017013613.1:c.8500G>T
|
XP_016869102.1:p.Glu2834Ter
|
|
NM_017780.4:c.8503G>T
MANE Select
|
NP_060250.2:p.Glu2835Ter
|
|