ENST00000248633.9:c.2755G>C
MANE Select
|
ENSP00000248633.4:p.Glu919Gln
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|
ENST00000248633.8:c.2755G>C
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ENSP00000248633.4:p.Glu919Gln
|
|
ENST00000428214.5:c.2584G>C
|
ENSP00000394413.1:p.Glu862Gln
|
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ENST00000438045.5:c.1789G>C
|
ENSP00000410438.1:p.Glu597Gln
|
|
ENST00000484913.5:n.2794G>C
|
|
|
ENST00000496420.5:n.2647G>C
|
|
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NM_000466.2:c.2755G>C
|
NP_000457.1:p.Glu919Gln
|
|
NM_001282677.1:c.2584G>C
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NP_001269606.1:p.Glu862Gln
|
|
NM_001282678.1:c.2131G>C
|
NP_001269607.1:p.Glu711Gln
|
|
XM_005250433.3:c.1006G>C
|
XP_005250490.1:p.Glu336Gln
|
|
XR_242246.3:n.2851G>C
|
|
|
XM_017012319.2:c.1006G>C
|
XP_016867808.1:p.Glu336Gln
|
|
XR_001744808.2:n.1782G>C
|
|
|
XR_242246.5:n.2802G>C
|
|
|
NM_000466.3:c.2755G>C
MANE Select
|
NP_000457.1:p.Glu919Gln
|
|
NM_001282677.2:c.2584G>C
|
NP_001269606.1:p.Glu862Gln
|
|
NM_001282678.2:c.2131G>C
|
NP_001269607.1:p.Glu711Gln
|
|