ENST00000695850.1:n.383A>G
|
|
|
ENST00000695853.1:c.*266A>G
|
ENSP00000512218.1:n.*266A>G
|
|
ENST00000423902.7:c.7207A>G
MANE Select
|
ENSP00000392028.1:p.Arg2403Gly
|
|
ENST00000423902.6:c.7207A>G
|
ENSP00000392028.1:p.Arg2403Gly
|
|
ENST00000524602.5:c.1717-5742A>G
|
ENSP00000437061.1:n.1717-5742A>G
|
|
ENST00000529472.1:n.388A>G
|
|
|
NM_001316690.1:c.1717-5742A>G
|
NP_001303619.1:n.1717-5742A>G
|
|
NM_017780.3:c.7207A>G
|
NP_060250.2:p.Arg2403Gly
|
|
XM_011517553.1:c.7297A>G
|
XP_011515855.1:p.Arg2433Gly
|
|
XM_011517554.1:c.7297A>G
|
XP_011515856.1:p.Arg2433Gly
|
|
XM_011517555.1:c.7294A>G
|
XP_011515857.1:p.Arg2432Gly
|
|
XM_011517556.1:c.7297A>G
|
XP_011515858.1:p.Arg2433Gly
|
|
XM_011517557.1:c.5284A>G
|
XP_011515859.1:p.Arg1762Gly
|
|
XM_011517558.1:c.4834A>G
|
XP_011515860.1:p.Arg1612Gly
|
|
XM_011517559.1:c.4042A>G
|
XP_011515861.1:p.Arg1348Gly
|
|
XM_011517553.2:c.7297A>G
|
XP_011515855.1:p.Arg2433Gly
|
|
XM_011517554.3:c.7297A>G
|
XP_011515856.1:p.Arg2433Gly
|
|
XM_011517555.2:c.7294A>G
|
XP_011515857.1:p.Arg2432Gly
|
|
XM_017013612.1:c.7297A>G
|
XP_016869101.1:p.Arg2433Gly
|
|
XM_017013613.1:c.7204A>G
|
XP_016869102.1:p.Arg2402Gly
|
|
NM_017780.4:c.7207A>G
MANE Select
|
NP_060250.2:p.Arg2403Gly
|
|