ENST00000248633.9:c.1786T>C
MANE Select
|
ENSP00000248633.4:p.Leu596=
|
|
ENST00000248633.8:c.1786T>C
|
ENSP00000248633.4:p.Leu596=
|
|
ENST00000422866.1:c.604T>C
|
|
|
ENST00000428214.5:c.1786T>C
|
ENSP00000394413.1:p.Leu596=
|
|
ENST00000438045.5:c.820T>C
|
ENSP00000410438.1:p.Leu274=
|
|
ENST00000484913.5:n.1825T>C
|
|
|
ENST00000496420.5:n.813T>C
|
|
|
NM_000466.2:c.1786T>C
|
NP_000457.1:p.Leu596=
|
|
NM_001282677.1:c.1786T>C
|
NP_001269606.1:p.Leu596=
|
|
NM_001282678.1:c.1162T>C
|
NP_001269607.1:p.Leu388=
|
|
XM_005250433.3:c.37T>C
|
XP_005250490.1:p.Leu13=
|
|
XR_242246.3:n.1882T>C
|
|
|
XM_017012319.2:c.37T>C
|
XP_016867808.1:p.Leu13=
|
|
XR_001744808.2:n.813T>C
|
|
|
XR_242246.5:n.1833T>C
|
|
|
NM_000466.3:c.1786T>C
MANE Select
|
NP_000457.1:p.Leu596=
|
|
NM_001282677.2:c.1786T>C
|
NP_001269606.1:p.Leu596=
|
|
NM_001282678.2:c.1162T>C
|
NP_001269607.1:p.Leu388=
|
|