ENST00000683572.1:n.593G>C
|
|
|
ENST00000341947.7:c.4787G>C
MANE Select
|
ENSP00000339915.2:p.Arg1596Pro
|
|
ENST00000341947.6:c.4787G>C
|
ENSP00000339915.2:p.Arg1596Pro
|
|
ENST00000361917.5:c.4466G>C
|
ENSP00000355123.1:p.Arg1489Pro
|
|
ENST00000374708.8:c.4529G>C
|
ENSP00000363840.4:p.Arg1510Pro
|
|
ENST00000477772.1:n.577G>C
|
|
|
NM_080679.2:c.4466G>C
|
NP_542410.2:p.Arg1489Pro
|
|
NM_080680.2:c.4787G>C
|
NP_542411.2:p.Arg1596Pro
|
|
NM_080681.2:c.4529G>C
|
NP_542412.2:p.Arg1510Pro
|
|
XM_011514298.1:c.3941G>C
|
XP_011512600.1:p.Arg1314Pro
|
|
XM_011514299.1:c.4073G>C
|
XP_011512601.1:p.Arg1358Pro
|
|
XM_011514300.1:c.3893G>C
|
XP_011512602.1:p.Arg1298Pro
|
|
XM_011514301.1:c.3830G>C
|
XP_011512603.1:p.Arg1277Pro
|
|
XM_011514302.1:c.3674G>C
|
XP_011512604.1:p.Arg1225Pro
|
|
XM_011514299.2:c.4073G>C
|
XP_011512601.1:p.Arg1358Pro
|
|
XM_011514300.2:c.3893G>C
|
XP_011512602.1:p.Arg1298Pro
|
|
XM_011514302.2:c.3674G>C
|
XP_011512604.1:p.Arg1225Pro
|
|
XM_017010250.1:c.4787G>C
|
XP_016865739.1:p.Arg1596Pro
|
|
XM_017010251.2:c.3605G>C
|
XP_016865740.1:p.Arg1202Pro
|
|
NM_080680.3:c.4787G>C
MANE Select
|
NP_542411.2:p.Arg1596Pro
|
|
NM_080681.3:c.4529G>C
|
NP_542412.2:p.Arg1510Pro
|
|
NM_080679.3:c.4466G>C
|
NP_542410.2:p.Arg1489Pro
|
|