ENST00000683572.1:n.787G>C
|
|
|
ENST00000341947.7:c.4981G>C
MANE Select
|
ENSP00000339915.2:p.Asp1661His
|
|
ENST00000341947.6:c.4981G>C
|
ENSP00000339915.2:p.Asp1661His
|
|
ENST00000361917.5:c.4660G>C
|
ENSP00000355123.1:p.Asp1554His
|
|
ENST00000374708.8:c.4723G>C
|
ENSP00000363840.4:p.Asp1575His
|
|
ENST00000477772.1:n.771G>C
|
|
|
NM_080679.2:c.4660G>C
|
NP_542410.2:p.Asp1554His
|
|
NM_080680.2:c.4981G>C
|
NP_542411.2:p.Asp1661His
|
|
NM_080681.2:c.4723G>C
|
NP_542412.2:p.Asp1575His
|
|
XM_011514298.1:c.4135G>C
|
XP_011512600.1:p.Asp1379His
|
|
XM_011514299.1:c.4267G>C
|
XP_011512601.1:p.Asp1423His
|
|
XM_011514300.1:c.4087G>C
|
XP_011512602.1:p.Asp1363His
|
|
XM_011514301.1:c.4024G>C
|
XP_011512603.1:p.Asp1342His
|
|
XM_011514302.1:c.3868G>C
|
XP_011512604.1:p.Asp1290His
|
|
XM_011514299.2:c.4267G>C
|
XP_011512601.1:p.Asp1423His
|
|
XM_011514300.2:c.4087G>C
|
XP_011512602.1:p.Asp1363His
|
|
XM_011514302.2:c.3868G>C
|
XP_011512604.1:p.Asp1290His
|
|
XM_017010250.1:c.4981G>C
|
XP_016865739.1:p.Asp1661His
|
|
XM_017010251.2:c.3799G>C
|
XP_016865740.1:p.Asp1267His
|
|
NM_080680.3:c.4981G>C
MANE Select
|
NP_542411.2:p.Asp1661His
|
|
NM_080681.3:c.4723G>C
|
NP_542412.2:p.Asp1575His
|
|
NM_080679.3:c.4660G>C
|
NP_542410.2:p.Asp1554His
|
|