ENST00000619189.5:c.280T>A
MANE Select
|
ENSP00000479542.1:p.Phe94Ile
|
|
ENST00000611685.4:c.167-9048T>A
|
|
|
ENST00000616848.4:c.6+4358T>A
|
ENSP00000480612.1:n.6+4358T>A
|
|
ENST00000619189.4:c.280T>A
|
ENSP00000479542.1:p.Phe94Ile
|
|
ENST00000619574.4:c.169-9048T>A
|
ENSP00000484706.1:n.169-9048T>A
|
|
ENST00000620553.2:n.336T>A
|
|
|
ENST00000620891.4:c.6+4358T>A
|
ENSP00000478019.1:n.6+4358T>A
|
|
NM_001163022.1:c.6+4358T>A
|
NP_001156494.1:n.6+4358T>A
|
|
NM_001163023.1:c.6+4358T>A
|
NP_001156495.1:n.6+4358T>A
|
|
NM_001276389.1:c.169-9048T>A
|
NP_001263318.1:n.169-9048T>A
|
|
NM_018474.4:c.280T>A
|
NP_060944.3:p.Phe94Ile
|
|
XM_011529296.1:c.280T>A
|
XP_011527598.1:p.Phe94Ile
|
|
XM_011529297.1:c.280T>A
|
XP_011527599.1:p.Phe94Ile
|
|
XM_011529298.1:c.280T>A
|
XP_011527600.1:p.Phe94Ile
|
|
XM_011529299.1:c.6+4358T>A
|
XP_011527601.1:n.6+4358T>A
|
|
XR_937105.1:n.404T>A
|
|
|
NM_001163022.2:c.6+4358T>A
|
NP_001156494.1:n.6+4358T>A
|
|
NM_001163023.2:c.6+4358T>A
|
NP_001156495.1:n.6+4358T>A
|
|
NM_001276389.2:c.169-9048T>A
|
NP_001263318.1:n.169-9048T>A
|
|
NM_001352434.1:c.280T>A
|
NP_001339363.1:p.Phe94Ile
|
|
NM_001352435.1:c.6+4358T>A
|
NP_001339364.1:n.6+4358T>A
|
|
NM_001352436.1:c.-107T>A
|
NP_001339365.1:n.-107T>A
|
|
NM_018474.5:c.280T>A
|
NP_060944.3:p.Phe94Ile
|
|
XM_011529296.3:c.280T>A
|
XP_011527598.1:p.Phe94Ile
|
|
XM_011529297.3:c.280T>A
|
XP_011527599.1:p.Phe94Ile
|
|
XM_011529299.3:c.6+4358T>A
|
XP_011527601.1:n.6+4358T>A
|
|
XM_017027951.2:c.-107T>A
|
XP_016883440.1:n.-107T>A
|
|
XM_017027952.2:c.6+4358T>A
|
XP_016883441.1:n.6+4358T>A
|
|
XR_001754334.2:n.346T>A
|
|
|
XR_937105.3:n.346T>A
|
|
|
NM_018474.6:c.280T>A
MANE Select
|
NP_060944.3:p.Phe94Ile
|
|
NM_001163022.3:c.6+4358T>A
|
NP_001156494.1:n.6+4358T>A
|
|
NM_001163023.3:c.6+4358T>A
|
NP_001156495.1:n.6+4358T>A
|
|
NM_001352434.2:c.280T>A
|
NP_001339363.1:p.Phe94Ile
|
|
NM_001352435.2:c.6+4358T>A
|
NP_001339364.1:n.6+4358T>A
|
|
NM_001352436.2:c.-107T>A
|
NP_001339365.1:n.-107T>A
|
|