ENST00000248633.9:c.1987G>C
MANE Select
|
ENSP00000248633.4:p.Asp663His
|
|
ENST00000248633.8:c.1987G>C
|
ENSP00000248633.4:p.Asp663His
|
|
ENST00000428214.5:c.1900+1432G>C
|
ENSP00000394413.1:n.1900+1432G>C
|
|
ENST00000438045.5:c.1021G>C
|
ENSP00000410438.1:p.Asp341His
|
|
ENST00000484913.5:n.2026G>C
|
|
|
ENST00000496420.5:n.1663G>C
|
|
|
NM_000466.2:c.1987G>C
|
NP_000457.1:p.Asp663His
|
|
NM_001282677.1:c.1900+1432G>C
|
NP_001269606.1:n.1900+1432G>C
|
|
NM_001282678.1:c.1363G>C
|
NP_001269607.1:p.Asp455His
|
|
XM_005250433.3:c.238G>C
|
XP_005250490.1:p.Asp80His
|
|
XR_242246.3:n.2083G>C
|
|
|
XM_017012319.2:c.238G>C
|
XP_016867808.1:p.Asp80His
|
|
XR_001744808.2:n.1014G>C
|
|
|
XR_242246.5:n.2034G>C
|
|
|
NM_000466.3:c.1987G>C
MANE Select
|
NP_000457.1:p.Asp663His
|
|
NM_001282677.2:c.1900+1432G>C
|
NP_001269606.1:n.1900+1432G>C
|
|
NM_001282678.2:c.1363G>C
|
NP_001269607.1:p.Asp455His
|
|