ENST00000681320.1:c.8298G>C
MANE Select
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ENSP00000506558.1:p.Gly2766=
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ENST00000328333.12:c.8298G>C
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ENSP00000332371.8:p.Gly2766=
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ENST00000474432.1:n.698G>C
|
|
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ENST00000487017.5:n.4937G>C
|
|
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NM_000094.3:c.8298G>C , LRG_286t1:c.8298G>C
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NP_000085.1:p.Gly2766=
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|
XM_011533336.1:c.8325G>C
|
XP_011531638.1:p.Gly2775=
|
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XM_011533337.1:c.8298G>C
|
XP_011531639.1:p.Gly2766=
|
|
XM_011533338.1:c.8265G>C
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XP_011531640.1:p.Gly2755=
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XR_940369.1:n.8361G>C
|
|
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XR_940370.1:n.8361G>C
|
|
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XR_940371.1:n.8361G>C
|
|
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XM_017005688.1:c.8238G>C
|
XP_016861177.1:p.Gly2746=
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XR_001740003.1:n.8334G>C
|
|
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XR_001740004.1:n.8334G>C
|
|
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XR_001740005.1:n.8334G>C
|
|
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NM_000094.4:c.8298G>C
MANE Select
|
NP_000085.1:p.Gly2766=
|
|