ENST00000405460.9:c.11382C>T
MANE Select
|
ENSP00000384582.2:p.Asn3794=
|
|
ENST00000425867.3:c.513C>T
|
ENSP00000392618.3:p.Asn171=
|
|
ENST00000639431.1:c.265+78778C>T
|
ENSP00000491057.1:n.265+78778C>T
|
|
ENST00000640374.1:n.4526C>T
|
|
|
ENST00000640464.1:n.1801C>T
|
|
|
ENST00000405460.6:c.11382C>T
|
ENSP00000384582.2:p.Asn3794=
|
|
ENST00000509621.1:c.4079C>T
|
|
|
NM_032119.3:c.11382C>T
|
NP_115495.3:p.Asn3794=
|
|
NR_003149.1:n.11395C>T
|
|
|
XM_011543675.1:c.11379C>T
|
XP_011541977.1:p.Asn3793=
|
|
XM_011543676.1:c.11301C>T
|
XP_011541978.1:p.Asn3767=
|
|
XM_011543677.1:c.8685C>T
|
XP_011541979.1:p.Asn2895=
|
|
XM_011543678.1:c.11382C>T
|
XP_011541980.1:p.Asn3794=
|
|
NM_032119.4:c.11382C>T
MANE Select
|
NP_115495.3:p.Asn3794=
|
|
XM_017009963.2:c.11403C>T
|
XP_016865452.1:p.Asn3801=
|
|
XM_017009964.2:c.11400C>T
|
XP_016865453.1:p.Asn3800=
|
|
XM_017009965.1:c.11400C>T
|
XP_016865454.1:p.Asn3800=
|
|
XM_017009966.2:c.11322C>T
|
XP_016865455.1:p.Asn3774=
|
|
XM_017009967.1:c.11307C>T
|
XP_016865456.1:p.Asn3769=
|
|
XM_017009968.2:c.11403C>T
|
XP_016865457.1:p.Asn3801=
|
|
XM_017009969.2:c.11403C>T
|
XP_016865458.1:p.Asn3801=
|
|
XM_017009970.2:c.11403C>T
|
XP_016865459.1:p.Asn3801=
|
|
XM_017009971.2:c.11403C>T
|
XP_016865460.1:p.Asn3801=
|
|
XM_017009972.1:c.4521C>T
|
XP_016865461.1:p.Asn1507=
|
|
XM_017009973.1:c.4500C>T
|
XP_016865462.1:p.Asn1500=
|
|
NR_003149.2:n.11398C>T
|
|
|