ENST00000220616.9:c.6745T>C
MANE Select
|
ENSP00000220616.4:p.Leu2249=
|
|
ENST00000220616.8:c.6745T>C
|
ENSP00000220616.4:p.Leu2249=
|
|
ENST00000518108.1:c.168+94T>C
|
|
|
ENST00000519178.5:c.2111T>C
|
|
|
ENST00000519543.5:c.1144T>C
|
ENSP00000430430.1:p.Leu382=
|
|
ENST00000522523.5:n.806T>C
|
|
|
ENST00000523756.5:c.3400T>C
|
|
|
NM_003235.4:c.6745T>C
|
NP_003226.4:p.Leu2249=
|
|
XM_005251038.3:c.6553T>C
|
XP_005251095.1:p.Leu2185=
|
|
XM_006716622.2:c.6682T>C
|
XP_006716685.1:p.Leu2228=
|
|
XM_005251038.4:c.6553T>C
|
XP_005251095.1:p.Leu2185=
|
|
XM_006716622.3:c.6682T>C
|
XP_006716685.1:p.Leu2228=
|
|
XM_017013793.1:c.6679T>C
|
XP_016869282.1:p.Leu2227=
|
|
XM_017013794.1:c.6745T>C
|
XP_016869283.1:p.Leu2249=
|
|
XM_017013795.1:c.6574T>C
|
XP_016869284.1:p.Leu2192=
|
|
XM_017013796.1:c.6526T>C
|
XP_016869285.1:p.Leu2176=
|
|
XM_017013797.1:c.6484T>C
|
XP_016869286.1:p.Leu2162=
|
|
XM_017013798.1:c.6745T>C
|
XP_016869287.1:p.Leu2249=
|
|
NM_003235.5:c.6745T>C
MANE Select
|
NP_003226.4:p.Leu2249=
|
|