ENST00000361917.6:c.554G>C
|
|
|
ENST00000341947.7:c.1981G>C
MANE Select
|
ENSP00000339915.2:p.Gly661Arg
|
|
ENST00000341947.6:c.1981G>C
|
ENSP00000339915.2:p.Gly661Arg
|
|
ENST00000361917.5:c.1660G>C
|
ENSP00000355123.1:p.Gly554Arg
|
|
ENST00000374708.8:c.1723G>C
|
ENSP00000363840.4:p.Gly575Arg
|
|
ENST00000477772.1:n.200G>C
|
|
|
NM_080679.2:c.1660G>C
|
NP_542410.2:p.Gly554Arg
|
|
NM_080680.2:c.1981G>C
|
NP_542411.2:p.Gly661Arg
|
|
NM_080681.2:c.1723G>C
|
NP_542412.2:p.Gly575Arg
|
|
XM_011514298.1:c.1135G>C
|
XP_011512600.1:p.Gly379Arg
|
|
XM_011514299.1:c.1267G>C
|
XP_011512601.1:p.Gly423Arg
|
|
XM_011514300.1:c.1087G>C
|
XP_011512602.1:p.Gly363Arg
|
|
XM_011514301.1:c.1024G>C
|
XP_011512603.1:p.Gly342Arg
|
|
XM_011514302.1:c.868G>C
|
XP_011512604.1:p.Gly290Arg
|
|
XM_011514299.2:c.1267G>C
|
XP_011512601.1:p.Gly423Arg
|
|
XM_011514300.2:c.1087G>C
|
XP_011512602.1:p.Gly363Arg
|
|
XM_011514302.2:c.868G>C
|
XP_011512604.1:p.Gly290Arg
|
|
XM_017010250.1:c.1981G>C
|
XP_016865739.1:p.Gly661Arg
|
|
XM_017010251.2:c.799G>C
|
XP_016865740.1:p.Gly267Arg
|
|
NM_080680.3:c.1981G>C
MANE Select
|
NP_542411.2:p.Gly661Arg
|
|
NM_080681.3:c.1723G>C
|
NP_542412.2:p.Gly575Arg
|
|
NM_080679.3:c.1660G>C
|
NP_542410.2:p.Gly554Arg
|
|