ENST00000220616.9:c.6028G=
MANE Select
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ENSP00000220616.4:p.Gly2010=
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ENST00000220616.8:c.6028G=
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ENSP00000220616.4:p.Gly2010=
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ENST00000519178.5:c.1394G=
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|
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ENST00000519294.5:n.20G=
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|
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ENST00000519543.5:c.490G=
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ENSP00000430430.1:p.Gly164=
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ENST00000520089.5:n.137G=
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ENST00000520197.5:n.165G=
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|
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ENST00000523756.5:c.2683G=
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NM_003235.4:c.6028G=
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NP_003226.4:p.Gly2010=
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XM_005251038.3:c.5836G=
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XP_005251095.1:p.Gly1946=
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XM_005251040.3:c.6028G=
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XP_005251097.1:p.Gly2010=
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XM_005251042.3:c.6028G=
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XP_005251099.1:p.Gly2010=
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|
XM_005251043.3:c.6028G=
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XP_005251100.1:p.Gly2010=
|
|
XM_006716622.2:c.6028G=
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XP_006716685.1:p.Gly2010=
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|
XM_005251038.4:c.5836G=
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XP_005251095.1:p.Gly1946=
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|
XM_005251040.4:c.6028G=
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XP_005251097.1:p.Gly2010=
|
|
XM_005251042.4:c.6028G=
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XP_005251099.1:p.Gly2010=
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|
XM_006716622.3:c.6028G=
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XP_006716685.1:p.Gly2010=
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|
XM_017013793.1:c.5962G=
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XP_016869282.1:p.Gly1988=
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|
XM_017013794.1:c.6028G=
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XP_016869283.1:p.Gly2010=
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|
XM_017013795.1:c.5857G=
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XP_016869284.1:p.Gly1953=
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XM_017013796.1:c.5809G=
|
XP_016869285.1:p.Gly1937=
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XM_017013797.1:c.5767G=
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XP_016869286.1:p.Gly1923=
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|
XM_017013798.1:c.6028G=
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XP_016869287.1:p.Gly2010=
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|
XM_017013799.1:c.6028G=
|
XP_016869288.1:p.Gly2010=
|
|
XM_017013800.1:c.6028G=
|
XP_016869289.1:p.Gly2010=
|
|
NM_003235.5:c.6028G=
MANE Select
|
NP_003226.4:p.Gly2010=
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