ENST00000683572.1:n.792T>C
|
|
|
ENST00000341947.7:c.4986T>C
MANE Select
|
ENSP00000339915.2:p.Gly1662=
|
|
ENST00000341947.6:c.4986T>C
|
ENSP00000339915.2:p.Gly1662=
|
|
ENST00000361917.5:c.4665T>C
|
ENSP00000355123.1:p.Gly1555=
|
|
ENST00000374708.8:c.4728T>C
|
ENSP00000363840.4:p.Gly1576=
|
|
ENST00000477772.1:n.776T>C
|
|
|
NM_080679.2:c.4665T>C
|
NP_542410.2:p.Gly1555=
|
|
NM_080680.2:c.4986T>C
|
NP_542411.2:p.Gly1662=
|
|
NM_080681.2:c.4728T>C
|
NP_542412.2:p.Gly1576=
|
|
XM_011514298.1:c.4140T>C
|
XP_011512600.1:p.Gly1380=
|
|
XM_011514299.1:c.4272T>C
|
XP_011512601.1:p.Gly1424=
|
|
XM_011514300.1:c.4092T>C
|
XP_011512602.1:p.Gly1364=
|
|
XM_011514301.1:c.4029T>C
|
XP_011512603.1:p.Gly1343=
|
|
XM_011514302.1:c.3873T>C
|
XP_011512604.1:p.Gly1291=
|
|
XM_011514299.2:c.4272T>C
|
XP_011512601.1:p.Gly1424=
|
|
XM_011514300.2:c.4092T>C
|
XP_011512602.1:p.Gly1364=
|
|
XM_011514302.2:c.3873T>C
|
XP_011512604.1:p.Gly1291=
|
|
XM_017010250.1:c.4986T>C
|
XP_016865739.1:p.Gly1662=
|
|
XM_017010251.2:c.3804T>C
|
XP_016865740.1:p.Gly1268=
|
|
NM_080680.3:c.4986T>C
MANE Select
|
NP_542411.2:p.Gly1662=
|
|
NM_080681.3:c.4728T>C
|
NP_542412.2:p.Gly1576=
|
|
NM_080679.3:c.4665T>C
|
NP_542410.2:p.Gly1555=
|
|