ENST00000220616.9:c.6745T>A
MANE Select
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ENSP00000220616.4:p.Leu2249Met
|
|
ENST00000220616.8:c.6745T>A
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ENSP00000220616.4:p.Leu2249Met
|
|
ENST00000518108.1:c.168+94T>A
|
|
|
ENST00000519178.5:c.2111T>A
|
|
|
ENST00000519543.5:c.1144T>A
|
ENSP00000430430.1:p.Leu382Met
|
|
ENST00000522523.5:n.806T>A
|
|
|
ENST00000523756.5:c.3400T>A
|
|
|
NM_003235.4:c.6745T>A
|
NP_003226.4:p.Leu2249Met
|
|
XM_005251038.3:c.6553T>A
|
XP_005251095.1:p.Leu2185Met
|
|
XM_006716622.2:c.6682T>A
|
XP_006716685.1:p.Leu2228Met
|
|
XM_005251038.4:c.6553T>A
|
XP_005251095.1:p.Leu2185Met
|
|
XM_006716622.3:c.6682T>A
|
XP_006716685.1:p.Leu2228Met
|
|
XM_017013793.1:c.6679T>A
|
XP_016869282.1:p.Leu2227Met
|
|
XM_017013794.1:c.6745T>A
|
XP_016869283.1:p.Leu2249Met
|
|
XM_017013795.1:c.6574T>A
|
XP_016869284.1:p.Leu2192Met
|
|
XM_017013796.1:c.6526T>A
|
XP_016869285.1:p.Leu2176Met
|
|
XM_017013797.1:c.6484T>A
|
XP_016869286.1:p.Leu2162Met
|
|
XM_017013798.1:c.6745T>A
|
XP_016869287.1:p.Leu2249Met
|
|
NM_003235.5:c.6745T>A
MANE Select
|
NP_003226.4:p.Leu2249Met
|
|