ENST00000324041.6:c.408C>T
MANE Select
|
ENSP00000326159.1:p.Ser136=
|
|
ENST00000324041.5:c.408C>T
|
ENSP00000326159.1:p.Ser136=
|
|
ENST00000431178.2:c.261C>T
|
ENSP00000399448.2:p.Ser87=
|
|
ENST00000593885.1:c.123C>T
|
ENSP00000469769.1:p.Ser41=
|
|
ENST00000596876.1:n.327C>T
|
|
|
ENST00000598305.5:c.123C>T
|
ENSP00000469963.1:p.Ser41=
|
|
ENST00000599865.5:n.261C>T
|
|
|
ENST00000602148.1:c.420C>T
|
ENSP00000472091.1:n.420C>T
|
|
NM_001302961.1:c.123C>T
|
NP_001289890.1:p.Ser41=
|
|
NM_004917.4:c.408C>T
|
NP_004908.4:p.Ser136=
|
|
NR_126566.1:n.401C>T
|
|
|
XM_005259441.3:c.123C>T
|
XP_005259498.2:p.Ser41=
|
|
XM_011527545.1:c.408C>T
|
XP_011525847.1:p.Ser136=
|
|
XM_011527546.1:c.408C>T
|
XP_011525848.1:p.Ser136=
|
|
XM_011527547.1:c.261C>T
|
XP_011525849.1:p.Ser87=
|
|
XM_005259441.4:c.123C>T
|
XP_005259498.2:p.Ser41=
|
|
XM_011527545.3:c.408C>T
|
XP_011525847.1:p.Ser136=
|
|
XM_011527546.2:c.408C>T
|
XP_011525848.1:p.Ser136=
|
|
NM_001302961.2:c.123C>T
|
NP_001289890.1:p.Ser41=
|
|
NR_126566.2:n.401C>T
|
|
|
NM_004917.5:c.408C>T
MANE Select
|
NP_004908.4:p.Ser136=
|
|