ENST00000349830.8:c.3411G>A
MANE Select
|
ENSP00000340297.3:p.Leu1137=
|
|
ENST00000635773.1:c.3939G>A
|
|
|
ENST00000635855.1:c.*3365G>A
|
ENSP00000489726.1:n.*3365G>A
|
|
ENST00000349830.7:c.3411G>A
|
ENSP00000340297.3:p.Leu1137=
|
|
ENST00000398564.5:c.3486G>A
|
ENSP00000381571.1:p.Leu1162=
|
|
ENST00000518288.5:c.3483G>A
|
ENSP00000431012.1:p.Leu1161=
|
|
ENST00000520359.5:c.3297G>A
|
ENSP00000427909.1:p.Leu1099=
|
|
ENST00000521927.1:n.248G>A
|
|
|
ENST00000522435.5:c.2343G>A
|
ENSP00000427768.1:p.Leu781=
|
|
ENST00000523596.5:n.503G>A
|
|
|
NM_001308152.1:c.3297G>A
|
NP_001295081.1:p.Leu1099=
|
|
NM_001308153.1:c.3483G>A
|
NP_001295082.1:p.Leu1161=
|
|
NM_014629.2:c.3411G>A , LRG_234t1:c.3411G>A
|
NP_055444.2:p.Leu1137=
|
|
NM_014629.3:c.3411G>A
|
NP_055444.2:p.Leu1137=
|
|
XM_005266041.2:c.3414G>A
|
XP_005266098.1:p.Leu1138=
|
|
XM_011534766.1:c.3327G>A
|
XP_011533068.1:p.Leu1109=
|
|
XM_011534767.1:c.3294G>A
|
XP_011533069.1:p.Leu1098=
|
|
XM_011534768.1:c.3401-4031G>A
|
XP_011533070.1:n.3401-4031G>A
|
|
XM_011534769.1:c.3369G>A
|
XP_011533071.1:p.Leu1123=
|
|
XM_005266041.4:c.3414G>A
|
XP_005266098.1:p.Leu1138=
|
|
XM_011534767.2:c.3294G>A
|
XP_011533069.1:p.Leu1098=
|
|
XM_017014003.1:c.3486G>A
|
XP_016869492.1:p.Leu1162=
|
|
XM_024447334.1:c.3414G>A
|
XP_024303102.1:p.Leu1138=
|
|
XM_024447335.1:c.3498G>A
|
XP_024303103.1:p.Leu1166=
|
|
NM_014629.4:c.3411G>A
MANE Select
|
NP_055444.2:p.Leu1137=
|
|
NM_001308152.2:c.3297G>A
|
NP_001295081.1:p.Leu1099=
|
|
NM_001308153.2:c.3483G>A
|
NP_001295082.1:p.Leu1161=
|
|