ENST00000397195.10:c.438T>G
MANE Select
|
ENSP00000380378.4:p.Leu146=
|
|
ENST00000674608.1:c.492T>G
|
ENSP00000501976.1:p.Leu164=
|
|
ENST00000674717.1:c.243T>G
|
ENSP00000501931.1:p.Leu81=
|
|
ENST00000675202.1:c.438T>G
|
ENSP00000502843.1:p.Leu146=
|
|
ENST00000675331.1:c.438T>G
|
ENSP00000502031.1:p.Leu146=
|
|
ENST00000675390.1:c.438T>G
|
ENSP00000501969.1:p.Leu146=
|
|
ENST00000675430.1:n.665T>G
|
|
|
ENST00000675621.1:c.438T>G
|
ENSP00000502117.1:p.Leu146=
|
|
ENST00000675764.1:c.*392T>G
|
ENSP00000502242.1:n.*392T>G
|
|
ENST00000676077.1:c.243T>G
|
ENSP00000502507.1:p.Leu81=
|
|
ENST00000676098.1:c.438T>G
|
ENSP00000502735.1:p.Leu146=
|
|
ENST00000676188.1:c.438T>G
|
ENSP00000502577.1:p.Leu146=
|
|
ENST00000676201.1:n.592T>G
|
|
|
ENST00000676353.1:c.243T>G
|
ENSP00000502737.1:p.Leu81=
|
|
ENST00000676456.1:n.543T>G
|
|
|
ENST00000397193.7:n.246T>G
|
|
|
ENST00000397195.9:c.438T>G
|
ENSP00000380378.4:p.Leu146=
|
|
ENST00000572915.6:n.480-74T>G
|
|
|
ENST00000574816.5:n.31-6113T>G
|
|
|
ENST00000609078.1:n.397T>G
|
|
|
NM_000430.3:c.438T>G
|
NP_000421.1:p.Leu146=
|
|
XM_011523901.1:c.492T>G
|
XP_011522203.1:p.Leu164=
|
|
XM_011523902.1:c.492T>G
|
XP_011522204.1:p.Leu164=
|
|
XM_011523903.1:c.492T>G
|
XP_011522205.1:p.Leu164=
|
|
XM_011523904.1:c.492T>G
|
XP_011522206.1:p.Leu164=
|
|
XM_011523901.2:c.492T>G
|
XP_011522203.1:p.Leu164=
|
|
XM_011523902.3:c.492T>G
|
XP_011522204.1:p.Leu164=
|
|
XM_011523903.2:c.492T>G
|
XP_011522205.1:p.Leu164=
|
|
XM_017024701.1:c.438T>G
|
XP_016880190.1:p.Leu146=
|
|
XM_017024702.2:c.243T>G
|
XP_016880191.1:p.Leu81=
|
|
NM_000430.4:c.438T>G
MANE Select
|
NP_000421.1:p.Leu146=
|
|