ENST00000248633.9:c.1895T>A
MANE Select
|
ENSP00000248633.4:p.Leu632Ter
|
|
ENST00000248633.8:c.1895T>A
|
ENSP00000248633.4:p.Leu632Ter
|
|
ENST00000422866.1:c.713T>A
|
|
|
ENST00000428214.5:c.1895T>A
|
ENSP00000394413.1:p.Leu632Ter
|
|
ENST00000438045.5:c.929T>A
|
ENSP00000410438.1:p.Leu310Ter
|
|
ENST00000484913.5:n.1934T>A
|
|
|
ENST00000496420.5:n.1571T>A
|
|
|
NM_000466.2:c.1895T>A
|
NP_000457.1:p.Leu632Ter
|
|
NM_001282677.1:c.1895T>A
|
NP_001269606.1:p.Leu632Ter
|
|
NM_001282678.1:c.1271T>A
|
NP_001269607.1:p.Leu424Ter
|
|
XM_005250433.3:c.146T>A
|
XP_005250490.1:p.Leu49Ter
|
|
XR_242246.3:n.1991T>A
|
|
|
XM_017012319.2:c.146T>A
|
XP_016867808.1:p.Leu49Ter
|
|
XR_001744808.2:n.922T>A
|
|
|
XR_242246.5:n.1942T>A
|
|
|
NM_000466.3:c.1895T>A
MANE Select
|
NP_000457.1:p.Leu632Ter
|
|
NM_001282677.2:c.1895T>A
|
NP_001269606.1:p.Leu632Ter
|
|
NM_001282678.2:c.1271T>A
|
NP_001269607.1:p.Leu424Ter
|
|