ENST00000695850.1:n.488C>T
|
|
|
ENST00000695853.1:c.*371C>T
|
ENSP00000512218.1:n.*371C>T
|
|
ENST00000423902.7:c.7312C>T
MANE Select
|
ENSP00000392028.1:p.Gln2438Ter
|
|
ENST00000423902.6:c.7312C>T
|
ENSP00000392028.1:p.Gln2438Ter
|
|
ENST00000524602.5:c.1717-5637C>T
|
ENSP00000437061.1:n.1717-5637C>T
|
|
ENST00000529472.1:n.493C>T
|
|
|
NM_001316690.1:c.1717-5637C>T
|
NP_001303619.1:n.1717-5637C>T
|
|
NM_017780.3:c.7312C>T
|
NP_060250.2:p.Gln2438Ter
|
|
XM_011517553.1:c.7402C>T
|
XP_011515855.1:p.Gln2468Ter
|
|
XM_011517554.1:c.7402C>T
|
XP_011515856.1:p.Gln2468Ter
|
|
XM_011517555.1:c.7399C>T
|
XP_011515857.1:p.Gln2467Ter
|
|
XM_011517556.1:c.7402C>T
|
XP_011515858.1:p.Gln2468Ter
|
|
XM_011517557.1:c.5389C>T
|
XP_011515859.1:p.Gln1797Ter
|
|
XM_011517558.1:c.4939C>T
|
XP_011515860.1:p.Gln1647Ter
|
|
XM_011517559.1:c.4147C>T
|
XP_011515861.1:p.Gln1383Ter
|
|
XM_011517553.2:c.7402C>T
|
XP_011515855.1:p.Gln2468Ter
|
|
XM_011517554.3:c.7402C>T
|
XP_011515856.1:p.Gln2468Ter
|
|
XM_011517555.2:c.7399C>T
|
XP_011515857.1:p.Gln2467Ter
|
|
XM_017013612.1:c.7402C>T
|
XP_016869101.1:p.Gln2468Ter
|
|
XM_017013613.1:c.7309C>T
|
XP_016869102.1:p.Gln2437Ter
|
|
NM_017780.4:c.7312C>T
MANE Select
|
NP_060250.2:p.Gln2438Ter
|
|