ENST00000683572.1:n.688G>C
|
|
|
ENST00000341947.7:c.4882G>C
MANE Select
|
ENSP00000339915.2:p.Glu1628Gln
|
|
ENST00000341947.6:c.4882G>C
|
ENSP00000339915.2:p.Glu1628Gln
|
|
ENST00000361917.5:c.4561G>C
|
ENSP00000355123.1:p.Glu1521Gln
|
|
ENST00000374708.8:c.4624G>C
|
ENSP00000363840.4:p.Glu1542Gln
|
|
ENST00000477772.1:n.672G>C
|
|
|
NM_080679.2:c.4561G>C
|
NP_542410.2:p.Glu1521Gln
|
|
NM_080680.2:c.4882G>C
|
NP_542411.2:p.Glu1628Gln
|
|
NM_080681.2:c.4624G>C
|
NP_542412.2:p.Glu1542Gln
|
|
XM_011514298.1:c.4036G>C
|
XP_011512600.1:p.Glu1346Gln
|
|
XM_011514299.1:c.4168G>C
|
XP_011512601.1:p.Glu1390Gln
|
|
XM_011514300.1:c.3988G>C
|
XP_011512602.1:p.Glu1330Gln
|
|
XM_011514301.1:c.3925G>C
|
XP_011512603.1:p.Glu1309Gln
|
|
XM_011514302.1:c.3769G>C
|
XP_011512604.1:p.Glu1257Gln
|
|
XM_011514299.2:c.4168G>C
|
XP_011512601.1:p.Glu1390Gln
|
|
XM_011514300.2:c.3988G>C
|
XP_011512602.1:p.Glu1330Gln
|
|
XM_011514302.2:c.3769G>C
|
XP_011512604.1:p.Glu1257Gln
|
|
XM_017010250.1:c.4882G>C
|
XP_016865739.1:p.Glu1628Gln
|
|
XM_017010251.2:c.3700G>C
|
XP_016865740.1:p.Glu1234Gln
|
|
NM_080680.3:c.4882G>C
MANE Select
|
NP_542411.2:p.Glu1628Gln
|
|
NM_080681.3:c.4624G>C
|
NP_542412.2:p.Glu1542Gln
|
|
NM_080679.3:c.4561G>C
|
NP_542410.2:p.Glu1521Gln
|
|