ENST00000308159.10:c.1162C>T
MANE Select
|
ENSP00000310668.5:p.Arg388Trp
|
|
ENST00000308159.9:c.1162C>T
|
ENSP00000310668.5:p.Arg388Trp
|
|
ENST00000542526.5:c.793C>T
|
ENSP00000440235.1:p.Arg265Trp
|
|
ENST00000563437.1:n.404C>T
|
|
|
ENST00000563858.5:c.541C>T
|
ENSP00000455230.1:p.Arg181Trp
|
|
ENST00000564887.5:c.793C>T
|
ENSP00000458039.1:p.Arg265Trp
|
|
ENST00000569842.5:c.1162C>T
|
ENSP00000458101.1:p.Arg388Trp
|
|
NM_001242795.1:c.793C>T
|
NP_001229724.1:p.Arg265Trp
|
|
NM_001242796.1:c.793C>T
|
NP_001229725.1:p.Arg265Trp
|
|
NM_014669.4:c.1162C>T
|
NP_055484.3:p.Arg388Trp
|
|
XM_005256263.2:c.1162C>T
|
XP_005256320.1:p.Arg388Trp
|
|
NM_001242796.2:c.793C>T
|
NP_001229725.1:p.Arg265Trp
|
|
XM_005256263.3:c.1162C>T
|
XP_005256320.1:p.Arg388Trp
|
|
NM_014669.5:c.1162C>T
MANE Select
|
NP_055484.3:p.Arg388Trp
|
|
NM_001242795.2:c.793C>T
|
NP_001229724.1:p.Arg265Trp
|
|