ENST00000348729.8:c.925T>C
MANE Select
|
ENSP00000302701.4:p.Cys309Arg
|
|
ENST00000348729.7:c.925T>C
|
ENSP00000302701.4:p.Cys309Arg
|
|
ENST00000353963.7:c.937T>C
|
ENSP00000302851.5:p.Cys313Arg
|
|
ENST00000504513.1:c.164+278T>C
|
|
|
ENST00000506512.1:n.536T>C
|
|
|
NM_005847.4:c.925T>C
|
NP_005838.3:p.Cys309Arg
|
|
NM_152685.3:c.937T>C
|
NP_689898.2:p.Cys313Arg
|
|
XM_005272148.3:c.1045T>C
|
XP_005272205.3:p.Cys349Arg
|
|
XM_005272149.3:c.1033T>C
|
XP_005272206.3:p.Cys345Arg
|
|
XM_006714741.2:c.1045T>C
|
XP_006714804.2:p.Cys349Arg
|
|
XM_011543765.1:c.1045T>C
|
XP_011542067.1:p.Cys349Arg
|
|
XM_011543766.1:c.826T>C
|
XP_011542068.1:p.Cys276Arg
|
|
XM_011543767.1:c.730T>C
|
XP_011542069.1:p.Cys244Arg
|
|
XM_011543768.1:c.610T>C
|
XP_011542070.1:p.Cys204Arg
|
|
XM_011543769.1:c.220T>C
|
XP_011542071.1:p.Cys74Arg
|
|
XM_005272149.4:c.1033T>C
|
XP_005272206.3:p.Cys345Arg
|
|
XM_011543765.2:c.1045T>C
|
XP_011542067.1:p.Cys349Arg
|
|
NM_005847.5:c.925T>C
MANE Select
|
NP_005838.3:p.Cys309Arg
|
|
NM_152685.4:c.937T>C
|
NP_689898.2:p.Cys313Arg
|
|