ENST00000248633.9:c.1973T>A
MANE Select
|
ENSP00000248633.4:p.Val658Asp
|
|
ENST00000248633.8:c.1973T>A
|
ENSP00000248633.4:p.Val658Asp
|
|
ENST00000428214.5:c.1900+1418T>A
|
ENSP00000394413.1:n.1900+1418T>A
|
|
ENST00000438045.5:c.1007T>A
|
ENSP00000410438.1:p.Val336Asp
|
|
ENST00000484913.5:n.2012T>A
|
|
|
ENST00000496420.5:n.1649T>A
|
|
|
NM_000466.2:c.1973T>A
|
NP_000457.1:p.Val658Asp
|
|
NM_001282677.1:c.1900+1418T>A
|
NP_001269606.1:n.1900+1418T>A
|
|
NM_001282678.1:c.1349T>A
|
NP_001269607.1:p.Val450Asp
|
|
XM_005250433.3:c.224T>A
|
XP_005250490.1:p.Val75Asp
|
|
XR_242246.3:n.2069T>A
|
|
|
XM_017012319.2:c.224T>A
|
XP_016867808.1:p.Val75Asp
|
|
XR_001744808.2:n.1000T>A
|
|
|
XR_242246.5:n.2020T>A
|
|
|
NM_000466.3:c.1973T>A
MANE Select
|
NP_000457.1:p.Val658Asp
|
|
NM_001282677.2:c.1900+1418T>A
|
NP_001269606.1:n.1900+1418T>A
|
|
NM_001282678.2:c.1349T>A
|
NP_001269607.1:p.Val450Asp
|
|