ENST00000248633.9:c.2749G>T
MANE Select
|
ENSP00000248633.4:p.Ala917Ser
|
|
ENST00000248633.8:c.2749G>T
|
ENSP00000248633.4:p.Ala917Ser
|
|
ENST00000428214.5:c.2578G>T
|
ENSP00000394413.1:p.Ala860Ser
|
|
ENST00000438045.5:c.1783G>T
|
ENSP00000410438.1:p.Ala595Ser
|
|
ENST00000484913.5:n.2788G>T
|
|
|
ENST00000496420.5:n.2641G>T
|
|
|
NM_000466.2:c.2749G>T
|
NP_000457.1:p.Ala917Ser
|
|
NM_001282677.1:c.2578G>T
|
NP_001269606.1:p.Ala860Ser
|
|
NM_001282678.1:c.2125G>T
|
NP_001269607.1:p.Ala709Ser
|
|
XM_005250433.3:c.1000G>T
|
XP_005250490.1:p.Ala334Ser
|
|
XR_242246.3:n.2845G>T
|
|
|
XM_017012319.2:c.1000G>T
|
XP_016867808.1:p.Ala334Ser
|
|
XR_001744808.2:n.1776G>T
|
|
|
XR_242246.5:n.2796G>T
|
|
|
NM_000466.3:c.2749G>T
MANE Select
|
NP_000457.1:p.Ala917Ser
|
|
NM_001282677.2:c.2578G>T
|
NP_001269606.1:p.Ala860Ser
|
|
NM_001282678.2:c.2125G>T
|
NP_001269607.1:p.Ala709Ser
|
|