ENST00000320185.7:c.201G>A
MANE Select
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ENSP00000321797.2:p.Glu67=
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|
ENST00000618991.5:c.-112G>A
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ENSP00000484420.1:n.-112G>A
|
|
ENST00000344255.8:c.168G>A
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ENSP00000340039.3:p.Glu56=
|
|
ENST00000320185.6:c.201G>A
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ENSP00000321797.2:p.Glu67=
|
|
ENST00000344255.7:c.168G>A
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ENSP00000340039.3:p.Glu56=
|
|
ENST00000346714.7:c.81G>A
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ENSP00000344306.3:p.Glu27=
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|
ENST00000347978.2:c.114G>A
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ENSP00000321945.2:p.Glu38=
|
|
ENST00000469792.6:c.*165G>A
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ENSP00000473299.1:n.*165G>A
|
|
ENST00000485728.1:n.77G>A
|
|
|
ENST00000618991.4:c.-112G>A
|
ENSP00000484420.1:n.-112G>A
|
|
NM_001206389.1:c.-112G>A
|
NP_001193318.1:n.-112G>A
|
|
NM_006119.4:c.114G>A
|
NP_006110.1:p.Glu38=
|
|
NM_033163.3:c.201G>A
|
NP_149353.1:p.Glu67=
|
|
NM_033164.3:c.168G>A
|
NP_149354.1:p.Glu56=
|
|
NM_033165.3:c.81G>A
|
NP_149355.1:p.Glu27=
|
|
XM_011539509.1:c.123G>A
|
XP_011537811.1:p.Glu41=
|
|
NM_006119.5:c.114G>A
|
NP_006110.1:p.Glu38=
|
|
NM_033163.4:c.201G>A
|
NP_149353.1:p.Glu67=
|
|
NM_033164.4:c.168G>A
|
NP_149354.1:p.Glu56=
|
|
NM_033165.4:c.81G>A
|
NP_149355.1:p.Glu27=
|
|
NM_001206389.2:c.-112G>A
|
NP_001193318.1:n.-112G>A
|
|
NM_006119.6:c.114G>A
|
NP_006110.1:p.Glu38=
|
|
NM_033163.5:c.201G>A
MANE Select
|
NP_149353.1:p.Glu67=
|
|
NM_033165.5:c.81G>A
|
NP_149355.1:p.Glu27=
|
|