ENST00000683572.1:n.606A>C
|
|
|
ENST00000341947.7:c.4800A>C
MANE Select
|
ENSP00000339915.2:p.Arg1600=
|
|
ENST00000341947.6:c.4800A>C
|
ENSP00000339915.2:p.Arg1600=
|
|
ENST00000361917.5:c.4479A>C
|
ENSP00000355123.1:p.Arg1493=
|
|
ENST00000374708.8:c.4542A>C
|
ENSP00000363840.4:p.Arg1514=
|
|
ENST00000477772.1:n.590A>C
|
|
|
NM_080679.2:c.4479A>C
|
NP_542410.2:p.Arg1493=
|
|
NM_080680.2:c.4800A>C
|
NP_542411.2:p.Arg1600=
|
|
NM_080681.2:c.4542A>C
|
NP_542412.2:p.Arg1514=
|
|
XM_011514298.1:c.3954A>C
|
XP_011512600.1:p.Arg1318=
|
|
XM_011514299.1:c.4086A>C
|
XP_011512601.1:p.Arg1362=
|
|
XM_011514300.1:c.3906A>C
|
XP_011512602.1:p.Arg1302=
|
|
XM_011514301.1:c.3843A>C
|
XP_011512603.1:p.Arg1281=
|
|
XM_011514302.1:c.3687A>C
|
XP_011512604.1:p.Arg1229=
|
|
XM_011514299.2:c.4086A>C
|
XP_011512601.1:p.Arg1362=
|
|
XM_011514300.2:c.3906A>C
|
XP_011512602.1:p.Arg1302=
|
|
XM_011514302.2:c.3687A>C
|
XP_011512604.1:p.Arg1229=
|
|
XM_017010250.1:c.4800A>C
|
XP_016865739.1:p.Arg1600=
|
|
XM_017010251.2:c.3618A>C
|
XP_016865740.1:p.Arg1206=
|
|
NM_080680.3:c.4800A>C
MANE Select
|
NP_542411.2:p.Arg1600=
|
|
NM_080681.3:c.4542A>C
|
NP_542412.2:p.Arg1514=
|
|
NM_080679.3:c.4479A>C
|
NP_542410.2:p.Arg1493=
|
|