ENST00000298171.7:c.905A>G
MANE Select
|
ENSP00000298171.2:p.Asn302Ser
|
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ENST00000636454.1:n.823A>G
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|
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ENST00000298171.6:c.905A>G
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ENSP00000298171.2:p.Asn302Ser
|
|
ENST00000541158.6:c.905A>G
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ENSP00000441235.2:p.Asn302Ser
|
|
NM_000369.2:c.905A>G , LRG_523t1:c.905A>G
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NP_000360.2:p.Asn302Ser
|
|
XM_005268037.3:c.905A>G
|
XP_005268094.1:p.Asn302Ser
|
|
XM_011537119.1:c.626A>G
|
XP_011535421.1:p.Asn209Ser
|
|
XR_245790.3:n.2086+22230T>C
|
|
|
XR_429385.2:n.853+22230T>C
|
|
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XR_429386.2:n.854+22230T>C
|
|
|
XR_944075.1:n.865+22230T>C
|
|
|
XR_944076.1:n.861+22230T>C
|
|
|
XR_944077.1:n.865+22230T>C
|
|
|
XR_944078.1:n.865+22230T>C
|
|
|
XR_944079.1:n.855+22230T>C
|
|
|
XM_005268037.4:c.905A>G
|
XP_005268094.1:p.Asn302Ser
|
|
XM_011537119.2:c.626A>G
|
XP_011535421.1:p.Asn209Ser
|
|
XR_001751021.1:n.2753+22230T>C
|
|
|
XR_001751022.1:n.2753+22230T>C
|
|
|
XR_001751023.1:n.2753+22230T>C
|
|
|
XR_944075.3:n.929+22230T>C
|
|
|
NM_000369.4:c.905A>G
|
NP_000360.2:p.Asn302Ser
|
|
NM_000369.5:c.905A>G
MANE Select
|
NP_000360.2:p.Asn302Ser
|
|