ENST00000380649.8:c.1118G>C
MANE Select
|
ENSP00000370023.3:p.Gly373Ala
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ENST00000492433.2:c.1118G>C
|
ENSP00000438039.2:p.Gly373Ala
|
|
ENST00000643057.1:c.*1009G>C
|
ENSP00000493761.1:n.*1009G>C
|
|
ENST00000643063.1:c.*164G>C
|
ENSP00000495353.1:n.*164G>C
|
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ENST00000643233.1:c.*1009G>C
|
ENSP00000493880.1:n.*1009G>C
|
|
ENST00000644428.1:c.1118G>C
|
ENSP00000495560.1:p.Gly373Ala
|
|
ENST00000645274.1:c.1013G>C
|
ENSP00000493996.1:p.Gly338Ala
|
|
ENST00000646031.1:c.477G>C
|
|
|
ENST00000646483.1:c.984G>C
|
ENSP00000496185.1:n.984G>C
|
|
ENST00000380649.7:c.1118G>C
|
ENSP00000370023.3:p.Gly373Ala
|
|
NM_000182.4:c.1118G>C
|
NP_000173.2:p.Gly373Ala
|
|
NM_000182.5:c.1118G>C
MANE Select
|
NP_000173.2:p.Gly373Ala
|
|