ENST00000352909.8:c.1045C>G
MANE Select
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ENSP00000325951.4:p.Gln349Glu
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ENST00000324155.8:c.*734C>G
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ENSP00000325831.3:n.*734C>G
|
|
ENST00000333684.9:c.763C>G
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ENSP00000328814.6:p.Gln255Glu
|
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ENST00000352909.7:c.1045C>G
|
ENSP00000325951.3:p.Gln349Glu
|
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ENST00000381168.7:c.*765C>G
|
ENSP00000370560.3:n.*765C>G
|
|
ENST00000381175.5:c.1126C>G
|
ENSP00000370567.1:p.Gln376Glu
|
|
ENST00000381178.5:c.1138C>G
|
ENSP00000370571.1:p.Gln380Glu
|
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ENST00000412076.1:c.203C>G
|
|
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ENST00000416223.5:c.339C>G
|
|
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ENST00000461172.1:n.210C>G
|
|
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ENST00000479437.5:n.594C>G
|
|
|
NM_000360.3:c.1045C>G
|
NP_000351.2:p.Gln349Glu
|
|
NM_199292.2:c.1138C>G
|
NP_954986.2:p.Gln380Glu
|
|
NM_199293.2:c.1126C>G
|
NP_954987.2:p.Gln376Glu
|
|
XM_011520335.1:c.1057C>G
|
XP_011518637.1:p.Gln353Glu
|
|
XM_011520335.2:c.1057C>G
|
XP_011518637.1:p.Gln353Glu
|
|
NM_000360.4:c.1045C>G
MANE Select
|
NP_000351.2:p.Gln349Glu
|
|
NM_199292.3:c.1138C>G
|
NP_954986.2:p.Gln380Glu
|
|
NM_199293.3:c.1126C>G
|
NP_954987.2:p.Gln376Glu
|
|