ENST00000248633.9:c.2085G>T
MANE Select
|
ENSP00000248633.4:p.Met695Ile
|
|
ENST00000248633.8:c.2085G>T
|
ENSP00000248633.4:p.Met695Ile
|
|
ENST00000428214.5:c.1914G>T
|
ENSP00000394413.1:p.Met638Ile
|
|
ENST00000438045.5:c.1119G>T
|
ENSP00000410438.1:p.Met373Ile
|
|
ENST00000484913.5:n.2124G>T
|
|
|
ENST00000496420.5:n.1761G>T
|
|
|
NM_000466.2:c.2085G>T
|
NP_000457.1:p.Met695Ile
|
|
NM_001282677.1:c.1914G>T
|
NP_001269606.1:p.Met638Ile
|
|
NM_001282678.1:c.1461G>T
|
NP_001269607.1:p.Met487Ile
|
|
XM_005250433.3:c.336G>T
|
XP_005250490.1:p.Met112Ile
|
|
XR_242246.3:n.2181G>T
|
|
|
XM_017012319.2:c.336G>T
|
XP_016867808.1:p.Met112Ile
|
|
XR_001744808.2:n.1112G>T
|
|
|
XR_242246.5:n.2132G>T
|
|
|
NM_000466.3:c.2085G>T
MANE Select
|
NP_000457.1:p.Met695Ile
|
|
NM_001282677.2:c.1914G>T
|
NP_001269606.1:p.Met638Ile
|
|
NM_001282678.2:c.1461G>T
|
NP_001269607.1:p.Met487Ile
|
|