ENST00000324464.8:c.1026G>T
MANE Select
|
ENSP00000315118.3:p.Leu342=
|
|
ENST00000593724.2:n.2849G>T
|
|
|
ENST00000594490.6:c.948G>T
|
ENSP00000471310.2:p.Leu316=
|
|
ENST00000594720.6:c.1026G>T
|
ENSP00000470876.2:p.Leu342=
|
|
ENST00000596455.6:n.1318G>T
|
|
|
ENST00000601967.6:c.1026G>T
|
ENSP00000470916.2:p.Leu342=
|
|
ENST00000676555.1:c.1026G>T
|
ENSP00000503387.1:p.Leu342=
|
|
ENST00000676578.1:c.*768G>T
|
ENSP00000504076.1:n.*768G>T
|
|
ENST00000676960.1:n.1151G>T
|
|
|
ENST00000676962.1:n.1305G>T
|
|
|
ENST00000677018.1:c.1026G>T
|
ENSP00000503480.1:p.Leu342=
|
|
ENST00000677039.1:n.3229G>T
|
|
|
ENST00000677399.1:n.1468G>T
|
|
|
ENST00000677496.1:c.699G>T
|
ENSP00000504773.1:p.Leu233=
|
|
ENST00000677517.1:c.699G>T
|
ENSP00000503519.1:p.Leu233=
|
|
ENST00000677633.1:c.*449G>T
|
ENSP00000503645.1:n.*449G>T
|
|
ENST00000677800.1:c.*4130G>T
|
ENSP00000503794.1:n.*4130G>T
|
|
ENST00000678057.1:c.*590G>T
|
ENSP00000503762.1:n.*590G>T
|
|
ENST00000678119.1:n.1220G>T
|
|
|
ENST00000678166.1:n.1169G>T
|
|
|
ENST00000678312.1:n.1363G>T
|
|
|
ENST00000678316.1:c.*449G>T
|
ENSP00000504112.1:n.*449G>T
|
|
ENST00000678371.1:n.1476G>T
|
|
|
ENST00000678404.1:c.1026G>T
|
ENSP00000503944.1:p.Leu342=
|
|
ENST00000678419.1:c.1026G>T
|
ENSP00000504085.1:p.Leu342=
|
|
ENST00000678433.1:n.1382G>T
|
|
|
ENST00000678467.1:c.1026G>T
|
ENSP00000504072.1:p.Leu342=
|
|
ENST00000678569.1:c.*11G>T
|
ENSP00000504261.1:n.*11G>T
|
|
ENST00000678961.1:n.1381G>T
|
|
|
ENST00000679002.1:n.1205G>T
|
|
|
ENST00000679012.1:c.582G>T
|
ENSP00000504446.1:p.Leu194=
|
|
ENST00000679070.1:c.*445G>T
|
ENSP00000503759.1:n.*445G>T
|
|
ENST00000679130.1:c.1026G>T
|
ENSP00000504845.1:p.Leu342=
|
|
ENST00000679315.1:c.*856G>T
|
ENSP00000503065.1:n.*856G>T
|
|
ENST00000243583.10:c.903G>T
|
ENSP00000243583.5:p.Leu301=
|
|
ENST00000324464.7:c.1026G>T
|
ENSP00000315118.3:p.Leu342=
|
|
ENST00000593724.1:n.1141G>T
|
|
|
NM_001142555.2:c.903G>T
|
NP_001136027.1:p.Leu301=
|
|
NM_024876.3:c.1026G>T
|
NP_079152.3:p.Leu342=
|
|
XM_005259270.3:c.1188G>T
|
XP_005259327.2:p.Leu396=
|
|
XM_005259271.3:c.1026G>T
|
XP_005259328.1:p.Leu342=
|
|
XM_005259272.3:c.1026G>T
|
XP_005259329.1:p.Leu342=
|
|
XM_005259273.3:c.1026G>T
|
XP_005259330.1:p.Leu342=
|
|
XM_006723392.2:c.1026G>T
|
XP_006723455.1:p.Leu342=
|
|
XM_006723393.2:c.1026G>T
|
XP_006723456.1:p.Leu342=
|
|
XM_011527334.1:c.1026G>T
|
XP_011525636.1:p.Leu342=
|
|
XM_011527335.1:c.885G>T
|
XP_011525637.1:p.Leu295=
|
|
XM_011527336.1:c.1056G>T
|
XP_011525638.1:p.Leu352=
|
|
XM_011527337.1:c.1026G>T
|
XP_011525639.1:p.Leu342=
|
|
XM_011527338.1:c.1026G>T
|
XP_011525640.1:p.Leu342=
|
|
NM_024876.4:c.1026G>T
MANE Select
|
NP_079152.3:p.Leu342=
|
|
NM_001142555.3:c.903G>T
|
NP_001136027.1:p.Leu301=
|
|