ENST00000695850.1:n.1532G=
|
|
|
ENST00000695852.1:n.463G=
|
|
|
ENST00000695853.1:c.*1415G=
|
ENSP00000512218.1:n.*1415G=
|
|
ENST00000423902.7:c.8356G=
MANE Select
|
ENSP00000392028.1:p.Gly2786=
|
|
ENST00000423902.6:c.8356G=
|
ENSP00000392028.1:p.Gly2786=
|
|
ENST00000524602.5:c.2209G=
|
ENSP00000437061.1:p.Gly737=
|
|
ENST00000528280.1:n.402G=
|
|
|
NM_001316690.1:c.2209G=
|
NP_001303619.1:p.Gly737=
|
|
NM_017780.3:c.8356G=
|
NP_060250.2:p.Gly2786=
|
|
XM_011517553.1:c.8446G=
|
XP_011515855.1:p.Gly2816=
|
|
XM_011517554.1:c.8446G=
|
XP_011515856.1:p.Gly2816=
|
|
XM_011517555.1:c.8443G=
|
XP_011515857.1:p.Gly2815=
|
|
XM_011517556.1:c.8224G=
|
XP_011515858.1:p.Gly2742=
|
|
XM_011517557.1:c.6433G=
|
XP_011515859.1:p.Gly2145=
|
|
XM_011517558.1:c.5983G=
|
XP_011515860.1:p.Gly1995=
|
|
XM_011517559.1:c.5191G=
|
XP_011515861.1:p.Gly1731=
|
|
XM_011517553.2:c.8446G=
|
XP_011515855.1:p.Gly2816=
|
|
XM_011517554.3:c.8446G=
|
XP_011515856.1:p.Gly2816=
|
|
XM_011517555.2:c.8443G=
|
XP_011515857.1:p.Gly2815=
|
|
XM_017013612.1:c.8446G=
|
XP_016869101.1:p.Gly2816=
|
|
XM_017013613.1:c.8353G=
|
XP_016869102.1:p.Gly2785=
|
|
NM_017780.4:c.8356G=
MANE Select
|
NP_060250.2:p.Gly2786=
|
|