ENST00000220616.9:c.6741G>T
MANE Select
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ENSP00000220616.4:p.Glu2247Asp
|
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ENST00000220616.8:c.6741G>T
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ENSP00000220616.4:p.Glu2247Asp
|
|
ENST00000518108.1:c.168+90G>T
|
|
|
ENST00000519178.5:c.2107G>T
|
|
|
ENST00000519543.5:c.1140G>T
|
ENSP00000430430.1:p.Glu380Asp
|
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ENST00000522523.5:n.802G>T
|
|
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ENST00000523756.5:c.3396G>T
|
|
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NM_003235.4:c.6741G>T
|
NP_003226.4:p.Glu2247Asp
|
|
XM_005251038.3:c.6549G>T
|
XP_005251095.1:p.Glu2183Asp
|
|
XM_006716622.2:c.6678G>T
|
XP_006716685.1:p.Glu2226Asp
|
|
XM_005251038.4:c.6549G>T
|
XP_005251095.1:p.Glu2183Asp
|
|
XM_006716622.3:c.6678G>T
|
XP_006716685.1:p.Glu2226Asp
|
|
XM_017013793.1:c.6675G>T
|
XP_016869282.1:p.Glu2225Asp
|
|
XM_017013794.1:c.6741G>T
|
XP_016869283.1:p.Glu2247Asp
|
|
XM_017013795.1:c.6570G>T
|
XP_016869284.1:p.Glu2190Asp
|
|
XM_017013796.1:c.6522G>T
|
XP_016869285.1:p.Glu2174Asp
|
|
XM_017013797.1:c.6480G>T
|
XP_016869286.1:p.Glu2160Asp
|
|
XM_017013798.1:c.6741G>T
|
XP_016869287.1:p.Glu2247Asp
|
|
NM_003235.5:c.6741G>T
MANE Select
|
NP_003226.4:p.Glu2247Asp
|
|