ENST00000394975.3:c.*155G=
MANE Select
|
ENSP00000378426.2:n.*155G=
|
|
ENST00000300851.10:c.*258G=
|
ENSP00000300851.6:n.*258G=
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|
ENST00000319788.11:c.*258G=
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ENSP00000326135.7:n.*258G=
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|
ENST00000354895.4:c.*258G=
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ENSP00000346969.4:n.*258G=
|
|
ENST00000394975.2:c.*155G=
|
ENSP00000378426.2:n.*155G=
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|
ENST00000420057.2:c.609G=
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|
|
ENST00000529564.1:c.283+2333G=
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ENSP00000431371.1:n.283+2333G=
|
|
ENST00000532364.1:c.173+3578G=
|
ENSP00000460316.1:n.173+3578G=
|
|
ENST00000533518.5:c.407+113G=
|
|
|
NM_001311311.1:c.*155G=
|
NP_001298240.1:n.*155G=
|
|
NM_024006.4:c.*155G=
|
NP_076869.1:n.*155G=
|
|
NM_024006.5:c.*155G=
|
NP_076869.1:n.*155G=
|
|
NM_206824.1:c.*258G=
|
NP_996560.1:n.*258G=
|
|
NM_206824.2:c.*258G=
|
NP_996560.1:n.*258G=
|
|
XM_011545944.1:c.*155G=
|
XP_011544246.1:n.*155G=
|
|
XM_011545945.1:c.*258G=
|
XP_011544247.1:n.*258G=
|
|
XR_950848.1:n.1435G=
|
|
|
NM_024006.6:c.*155G=
MANE Select
|
NP_076869.1:n.*155G=
|
|
NM_001311311.2:c.*155G=
|
NP_001298240.1:n.*155G=
|
|
NM_206824.3:c.*258G=
|
NP_996560.1:n.*258G=
|
|