ENST00000681320.1:c.7989G>A
MANE Select
|
ENSP00000506558.1:p.Glu2663=
|
|
ENST00000328333.12:c.7989G>A
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ENSP00000332371.8:p.Glu2663=
|
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ENST00000487017.5:n.4628G>A
|
|
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NM_000094.3:c.7989G>A , LRG_286t1:c.7989G>A
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NP_000085.1:p.Glu2663=
|
|
XM_011533336.1:c.8016G>A
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XP_011531638.1:p.Glu2672=
|
|
XM_011533337.1:c.7989G>A
|
XP_011531639.1:p.Glu2663=
|
|
XM_011533338.1:c.7956G>A
|
XP_011531640.1:p.Glu2652=
|
|
XR_940369.1:n.8052G>A
|
|
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XR_940370.1:n.8052G>A
|
|
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XR_940371.1:n.8052G>A
|
|
|
XM_017005688.1:c.7929G>A
|
XP_016861177.1:p.Glu2643=
|
|
XR_001740003.1:n.8025G>A
|
|
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XR_001740004.1:n.8025G>A
|
|
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XR_001740005.1:n.8025G>A
|
|
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NM_000094.4:c.7989G>A
MANE Select
|
NP_000085.1:p.Glu2663=
|
|