ENST00000220616.9:c.5995C>T
MANE Select
|
ENSP00000220616.4:p.Arg1999Trp
|
|
ENST00000220616.8:c.5995C>T
|
ENSP00000220616.4:p.Arg1999Trp
|
|
ENST00000519178.5:c.1361C>T
|
|
|
ENST00000519543.5:c.457C>T
|
ENSP00000430430.1:p.Arg153Trp
|
|
ENST00000520089.5:n.104C>T
|
|
|
ENST00000520197.5:n.132C>T
|
|
|
ENST00000523756.5:c.2650C>T
|
|
|
NM_003235.4:c.5995C>T
|
NP_003226.4:p.Arg1999Trp
|
|
XM_005251038.3:c.5803C>T
|
XP_005251095.1:p.Arg1935Trp
|
|
XM_005251040.3:c.5995C>T
|
XP_005251097.1:p.Arg1999Trp
|
|
XM_005251042.3:c.5995C>T
|
XP_005251099.1:p.Arg1999Trp
|
|
XM_005251043.3:c.5995C>T
|
XP_005251100.1:p.Arg1999Trp
|
|
XM_006716622.2:c.5995C>T
|
XP_006716685.1:p.Arg1999Trp
|
|
XM_005251038.4:c.5803C>T
|
XP_005251095.1:p.Arg1935Trp
|
|
XM_005251040.4:c.5995C>T
|
XP_005251097.1:p.Arg1999Trp
|
|
XM_005251042.4:c.5995C>T
|
XP_005251099.1:p.Arg1999Trp
|
|
XM_006716622.3:c.5995C>T
|
XP_006716685.1:p.Arg1999Trp
|
|
XM_017013793.1:c.5929C>T
|
XP_016869282.1:p.Arg1977Trp
|
|
XM_017013794.1:c.5995C>T
|
XP_016869283.1:p.Arg1999Trp
|
|
XM_017013795.1:c.5824C>T
|
XP_016869284.1:p.Arg1942Trp
|
|
XM_017013796.1:c.5776C>T
|
XP_016869285.1:p.Arg1926Trp
|
|
XM_017013797.1:c.5734C>T
|
XP_016869286.1:p.Arg1912Trp
|
|
XM_017013798.1:c.5995C>T
|
XP_016869287.1:p.Arg1999Trp
|
|
XM_017013799.1:c.5995C>T
|
XP_016869288.1:p.Arg1999Trp
|
|
XM_017013800.1:c.5995C>T
|
XP_016869289.1:p.Arg1999Trp
|
|
NM_003235.5:c.5995C>T
MANE Select
|
NP_003226.4:p.Arg1999Trp
|
|