ENST00000248633.9:c.1938G>C
MANE Select
|
ENSP00000248633.4:p.Val646=
|
|
ENST00000248633.8:c.1938G>C
|
ENSP00000248633.4:p.Val646=
|
|
ENST00000428214.5:c.1900+1383G>C
|
ENSP00000394413.1:n.1900+1383G>C
|
|
ENST00000438045.5:c.972G>C
|
ENSP00000410438.1:p.Val324=
|
|
ENST00000484913.5:n.1977G>C
|
|
|
ENST00000496420.5:n.1614G>C
|
|
|
NM_000466.2:c.1938G>C
|
NP_000457.1:p.Val646=
|
|
NM_001282677.1:c.1900+1383G>C
|
NP_001269606.1:n.1900+1383G>C
|
|
NM_001282678.1:c.1314G>C
|
NP_001269607.1:p.Val438=
|
|
XM_005250433.3:c.189G>C
|
XP_005250490.1:p.Val63=
|
|
XR_242246.3:n.2034G>C
|
|
|
XM_017012319.2:c.189G>C
|
XP_016867808.1:p.Val63=
|
|
XR_001744808.2:n.965G>C
|
|
|
XR_242246.5:n.1985G>C
|
|
|
NM_000466.3:c.1938G>C
MANE Select
|
NP_000457.1:p.Val646=
|
|
NM_001282677.2:c.1900+1383G>C
|
NP_001269606.1:n.1900+1383G>C
|
|
NM_001282678.2:c.1314G>C
|
NP_001269607.1:p.Val438=
|
|