ENST00000265631.10:c.1309T>C
MANE Select
|
ENSP00000265631.6:p.Cys437Arg
|
|
ENST00000265631.9:c.1309T>C
|
ENSP00000265631.5:p.Cys437Arg
|
|
ENST00000416240.6:c.1312T>C
|
ENSP00000400101.2:p.Cys438Arg
|
|
ENST00000484495.5:n.462T>C
|
|
|
ENST00000490072.5:n.376T>C
|
|
|
ENST00000492869.1:n.430T>C
|
|
|
NM_001160210.1:c.1312T>C
|
NP_001153682.1:p.Cys438Arg
|
|
NM_014251.2:c.1309T>C
|
NP_055066.1:p.Cys437Arg
|
|
NR_027662.1:n.1384T>C
|
|
|
XM_006715831.2:c.1342T>C
|
XP_006715894.1:p.Cys448Arg
|
|
XM_011515727.1:c.1342T>C
|
XP_011514029.1:p.Cys448Arg
|
|
XM_011515728.1:c.457T>C
|
XP_011514030.1:p.Cys153Arg
|
|
XM_006715831.4:c.1342T>C
|
XP_006715894.1:p.Cys448Arg
|
|
XM_011515727.3:c.1342T>C
|
XP_011514029.1:p.Cys448Arg
|
|
XM_017011663.1:c.1300T>C
|
XP_016867152.1:p.Cys434Arg
|
|
XM_017011664.2:c.457T>C
|
XP_016867153.1:p.Cys153Arg
|
|
XM_017011665.1:c.457T>C
|
XP_016867154.1:p.Cys153Arg
|
|
XR_001744525.2:n.1480T>C
|
|
|
XR_002956405.1:n.2113T>C
|
|
|
NM_014251.3:c.1309T>C
MANE Select
|
NP_055066.1:p.Cys437Arg
|
|
NR_027662.2:n.1335T>C
|
|
|
NM_001160210.2:c.1312T>C
|
NP_001153682.1:p.Cys438Arg
|
|