|
ENST00000375687.10:c.3403C>T
MANE Select
|
ENSP00000364839.4:p.Gln1135Ter
|
|
|
ENST00000646985.1:c.3220C>T
|
ENSP00000495053.1:p.Gln1074Ter
|
|
|
ENST00000647223.1:n.5756C>T
|
|
|
|
ENST00000651418.1:c.1869+1534C>T
|
ENSP00000499150.1:n.1869+1534C>T
|
|
|
ENST00000306058.9:c.3388C>T
|
ENSP00000305119.5:p.Gln1130Ter
|
|
|
ENST00000375687.8:c.3403C>T
|
ENSP00000364839.4:p.Gln1135Ter
|
|
|
ENST00000613218.4:c.3403C>T
|
ENSP00000480487.1:p.Gln1135Ter
|
|
|
ENST00000620121.4:c.3403C>T
|
ENSP00000481978.1:p.Gln1135Ter
|
|
|
NM_015338.5:c.3403C>T , LRG_630t1:c.3403C>T
|
NP_056153.2:p.Gln1135Ter
|
|
|
XM_006723727.2:c.3400C>T
|
XP_006723790.1:p.Gln1134Ter
|
|
|
XM_006723728.2:c.3373C>T
|
XP_006723791.1:p.Gln1125Ter
|
|
|
XM_006723730.2:c.3319C>T
|
XP_006723793.1:p.Gln1107Ter
|
|
|
XM_006723732.2:c.3220C>T
|
XP_006723795.1:p.Gln1074Ter
|
|
|
XM_006723733.1:c.2719C>T
|
XP_006723796.1:p.Gln907Ter
|
|
|
XM_011528647.1:c.3667C>T
|
XP_011526949.1:p.Gln1223Ter
|
|
|
XM_011528648.1:c.3664C>T
|
XP_011526950.1:p.Gln1222Ter
|
|
|
XM_011528649.1:c.3583C>T
|
XP_011526951.1:p.Gln1195Ter
|
|
|
XM_011528650.1:c.3514C>T
|
XP_011526952.1:p.Gln1172Ter
|
|
|
XM_011528651.1:c.3382C>T
|
XP_011526953.1:p.Gln1128Ter
|
|
|
XM_011528652.1:c.3319C>T
|
XP_011526954.1:p.Gln1107Ter
|
|
|
NM_001363734.1:c.3220C>T
|
NP_001350663.1:p.Gln1074Ter
|
|
|
XM_006723727.3:c.3400C>T
|
XP_006723790.1:p.Gln1134Ter
|
|
|
XM_006723728.3:c.3373C>T
|
XP_006723791.1:p.Gln1125Ter
|
|
|
XM_006723730.4:c.3319C>T
|
XP_006723793.1:p.Gln1107Ter
|
|
|
XM_011528648.3:c.3664C>T
|
XP_011526950.1:p.Gln1222Ter
|
|
|
XM_011528652.2:c.3319C>T
|
XP_011526954.1:p.Gln1107Ter
|
|
|
XM_017027704.1:c.3319C>T
|
XP_016883193.1:p.Gln1107Ter
|
|
|
XM_017027705.1:c.3319C>T
|
XP_016883194.1:p.Gln1107Ter
|
|
|
XM_017027706.1:c.3250C>T
|
XP_016883195.1:p.Gln1084Ter
|
|
|
NM_015338.6:c.3403C>T
MANE Select
|
NP_056153.2:p.Gln1135Ter
|
|
