ENST00000290866.10:c.3896C=
MANE Select
|
ENSP00000290866.4:p.Ser1299=
|
|
ENST00000290863.10:c.2174C=
|
ENSP00000290863.6:p.Ser725=
|
|
ENST00000290866.9:c.3896C=
|
ENSP00000290866.4:p.Ser1299=
|
|
ENST00000413513.7:c.2051C=
|
ENSP00000392247.3:p.Ser684=
|
|
ENST00000428043.5:c.*318C=
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ENSP00000397593.2:n.*318C=
|
|
ENST00000577647.2:c.1969+356C=
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ENSP00000464149.1:n.1969+356C=
|
|
ENST00000578839.5:c.*1651C=
|
ENSP00000462110.2:n.*1651C=
|
|
ENST00000579314.5:c.*1625C=
|
ENSP00000462599.1:n.*1625C=
|
|
NM_000789.3:c.3896C=
|
NP_000780.1:p.Ser1299=
|
|
NM_001178057.1:c.2051C=
|
NP_001171528.1:p.Ser684=
|
|
NM_152830.2:c.2174C=
|
NP_690043.1:p.Ser725=
|
|
XM_005257110.1:c.3347C=
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XP_005257167.1:p.Ser1116=
|
|
XM_006721737.2:c.2234C=
|
XP_006721800.2:p.Ser745=
|
|
XM_006721737.3:c.2234C=
|
XP_006721800.2:p.Ser745=
|
|
NM_000789.4:c.3896C=
MANE Select
|
NP_000780.1:p.Ser1299=
|
|
NM_001178057.2:c.2051C=
|
NP_001171528.1:p.Ser684=
|
|
NM_152830.3:c.2174C=
|
NP_690043.1:p.Ser725=
|
|
NM_001382700.1:c.3329C=
|
NP_001369629.1:p.Ser1110=
|
|
NM_001382701.1:c.3044C=
|
NP_001369630.1:p.Ser1015=
|
|
NM_001382702.1:c.1511C=
|
NP_001369631.1:p.Ser504=
|
|
NR_168483.1:n.2274C=
|
|
|