ENST00000308159.10:c.1814C>G
MANE Select
|
ENSP00000310668.5:p.Thr605Arg
|
|
ENST00000308159.9:c.1814C>G
|
ENSP00000310668.5:p.Thr605Arg
|
|
ENST00000542526.5:c.1445C>G
|
ENSP00000440235.1:p.Thr482Arg
|
|
ENST00000563405.1:c.8C>G
|
ENSP00000458078.1:p.Thr3Arg
|
|
ENST00000564887.5:c.1445C>G
|
ENSP00000458039.1:p.Thr482Arg
|
|
ENST00000569842.5:c.1814C>G
|
ENSP00000458101.1:p.Thr605Arg
|
|
NM_001242795.1:c.1445C>G
|
NP_001229724.1:p.Thr482Arg
|
|
NM_001242796.1:c.1445C>G
|
NP_001229725.1:p.Thr482Arg
|
|
NM_014669.4:c.1814C>G
|
NP_055484.3:p.Thr605Arg
|
|
XM_005256263.2:c.1814C>G
|
XP_005256320.1:p.Thr605Arg
|
|
NM_001242796.2:c.1445C>G
|
NP_001229725.1:p.Thr482Arg
|
|
XM_005256263.3:c.1814C>G
|
XP_005256320.1:p.Thr605Arg
|
|
NM_014669.5:c.1814C>G
MANE Select
|
NP_055484.3:p.Thr605Arg
|
|
NM_001242795.2:c.1445C>G
|
NP_001229724.1:p.Thr482Arg
|
|