ENST00000683572.1:n.754G>C
|
|
|
ENST00000341947.7:c.4948G>C
MANE Select
|
ENSP00000339915.2:p.Asp1650His
|
|
ENST00000341947.6:c.4948G>C
|
ENSP00000339915.2:p.Asp1650His
|
|
ENST00000361917.5:c.4627G>C
|
ENSP00000355123.1:p.Asp1543His
|
|
ENST00000374708.8:c.4690G>C
|
ENSP00000363840.4:p.Asp1564His
|
|
ENST00000477772.1:n.738G>C
|
|
|
NM_080679.2:c.4627G>C
|
NP_542410.2:p.Asp1543His
|
|
NM_080680.2:c.4948G>C
|
NP_542411.2:p.Asp1650His
|
|
NM_080681.2:c.4690G>C
|
NP_542412.2:p.Asp1564His
|
|
XM_011514298.1:c.4102G>C
|
XP_011512600.1:p.Asp1368His
|
|
XM_011514299.1:c.4234G>C
|
XP_011512601.1:p.Asp1412His
|
|
XM_011514300.1:c.4054G>C
|
XP_011512602.1:p.Asp1352His
|
|
XM_011514301.1:c.3991G>C
|
XP_011512603.1:p.Asp1331His
|
|
XM_011514302.1:c.3835G>C
|
XP_011512604.1:p.Asp1279His
|
|
XM_011514299.2:c.4234G>C
|
XP_011512601.1:p.Asp1412His
|
|
XM_011514300.2:c.4054G>C
|
XP_011512602.1:p.Asp1352His
|
|
XM_011514302.2:c.3835G>C
|
XP_011512604.1:p.Asp1279His
|
|
XM_017010250.1:c.4948G>C
|
XP_016865739.1:p.Asp1650His
|
|
XM_017010251.2:c.3766G>C
|
XP_016865740.1:p.Asp1256His
|
|
NM_080680.3:c.4948G>C
MANE Select
|
NP_542411.2:p.Asp1650His
|
|
NM_080681.3:c.4690G>C
|
NP_542412.2:p.Asp1564His
|
|
NM_080679.3:c.4627G>C
|
NP_542410.2:p.Asp1543His
|
|