ENST00000289473.11:c.1061G>T
MANE Select
|
ENSP00000289473.4:p.Arg354Leu
|
|
ENST00000289473.10:c.1061G>T
|
ENSP00000289473.4:p.Arg354Leu
|
|
ENST00000289473.8:c.1061G>T
|
ENSP00000289473.4:p.Arg354Leu
|
|
ENST00000398421.6:n.2088G>T
|
|
|
ENST00000455062.2:n.1170G>T
|
|
|
NM_000265.5:c.1061G>T
|
NP_000256.4:p.Arg354Leu
|
|
XM_005250543.3:c.1023G>T
|
XP_005250600.2:p.Ala341=
|
|
XM_011516498.1:c.1060G>T
|
XP_011514800.1:p.Gly354Cys
|
|
XM_011516501.1:c.668G>T
|
XP_011514803.1:p.Arg223Leu
|
|
NM_000265.6:c.1061G>T
|
NP_000256.4:p.Arg354Leu
|
|
NM_000265.7:c.1061G>T
MANE Select
|
NP_000256.4:p.Arg354Leu
|
|