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ENST00000389817.8:c.4545G=
MANE Select
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ENST00000642271.1:c.4542G=
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NM_000352.4:c.4545G=
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NP_000343.2:p.Thr1515=
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NM_001287174.1:c.4548G=
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NP_001274103.1:p.Thr1516=
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XM_011520331.1:c.4545G=
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XP_011518633.1:p.Thr1515=
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XM_011520332.1:c.*10G=
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XP_011518634.1:n.*10G=
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XM_011520333.1:c.3045G=
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XP_011518635.1:p.Thr1015=
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XR_930890.1:n.4507G=
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NM_001351295.1:c.4611G=
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NP_001338224.1:p.Thr1537=
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NM_001351296.1:c.4545G=
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NP_001338225.1:p.Thr1515=
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NM_001351297.1:c.4542G=
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NP_001338226.1:p.Thr1514=
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NR_147094.1:n.4840G=
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XM_017018197.2:c.4614G=
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XP_016873686.1:p.Thr1538=
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XM_017018199.1:c.4611G=
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XP_016873688.1:p.Thr1537=
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XM_017018201.2:c.*10G=
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XP_016873690.1:n.*10G=
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XM_017018202.1:c.3111G=
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XP_016873691.1:p.Thr1037=
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XM_017018204.1:c.2502G=
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XP_016873693.1:p.Thr834=
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XM_024448668.1:c.2913G=
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XP_024304436.1:p.Thr971=
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XR_001747945.2:n.4582G=
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XR_001747946.2:n.4513G=
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XR_002957189.1:n.6296G=
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NM_000352.6:c.4545G=
MANE Select
|
NP_000343.2:p.Thr1515=
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NM_001287174.2:c.4548G=
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NP_001274103.1:p.Thr1516=
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NM_001351295.2:c.4611G=
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NP_001338224.1:p.Thr1537=
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NM_001351296.2:c.4545G=
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NP_001338225.1:p.Thr1515=
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NM_001351297.2:c.4542G=
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NP_001338226.1:p.Thr1514=
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NR_147094.2:n.4840G=
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NM_001287174.3:c.4548G=
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NP_001274103.1:p.Thr1516=
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