ENST00000248633.9:c.2276G>A
MANE Select
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ENSP00000248633.4:p.Cys759Tyr
|
|
ENST00000248633.8:c.2276G>A
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ENSP00000248633.4:p.Cys759Tyr
|
|
ENST00000428214.5:c.2105G>A
|
ENSP00000394413.1:p.Cys702Tyr
|
|
ENST00000438045.5:c.1310G>A
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ENSP00000410438.1:p.Cys437Tyr
|
|
ENST00000484913.5:n.2315G>A
|
|
|
ENST00000496092.1:n.74G>A
|
|
|
ENST00000496420.5:n.1952G>A
|
|
|
NM_000466.2:c.2276G>A
|
NP_000457.1:p.Cys759Tyr
|
|
NM_001282677.1:c.2105G>A
|
NP_001269606.1:p.Cys702Tyr
|
|
NM_001282678.1:c.1652G>A
|
NP_001269607.1:p.Cys551Tyr
|
|
XM_005250433.3:c.527G>A
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XP_005250490.1:p.Cys176Tyr
|
|
XR_242246.3:n.2372G>A
|
|
|
XM_017012319.2:c.527G>A
|
XP_016867808.1:p.Cys176Tyr
|
|
XR_001744808.2:n.1303G>A
|
|
|
XR_242246.5:n.2323G>A
|
|
|
NM_000466.3:c.2276G>A
MANE Select
|
NP_000457.1:p.Cys759Tyr
|
|
NM_001282677.2:c.2105G>A
|
NP_001269606.1:p.Cys702Tyr
|
|
NM_001282678.2:c.1652G>A
|
NP_001269607.1:p.Cys551Tyr
|
|