ENST00000683572.1:n.669G>T
|
|
|
ENST00000341947.7:c.4863G>T
MANE Select
|
ENSP00000339915.2:p.Gln1621His
|
|
ENST00000341947.6:c.4863G>T
|
ENSP00000339915.2:p.Gln1621His
|
|
ENST00000361917.5:c.4542G>T
|
ENSP00000355123.1:p.Gln1514His
|
|
ENST00000374708.8:c.4605G>T
|
ENSP00000363840.4:p.Gln1535His
|
|
ENST00000477772.1:n.653G>T
|
|
|
NM_080679.2:c.4542G>T
|
NP_542410.2:p.Gln1514His
|
|
NM_080680.2:c.4863G>T
|
NP_542411.2:p.Gln1621His
|
|
NM_080681.2:c.4605G>T
|
NP_542412.2:p.Gln1535His
|
|
XM_011514298.1:c.4017G>T
|
XP_011512600.1:p.Gln1339His
|
|
XM_011514299.1:c.4149G>T
|
XP_011512601.1:p.Gln1383His
|
|
XM_011514300.1:c.3969G>T
|
XP_011512602.1:p.Gln1323His
|
|
XM_011514301.1:c.3906G>T
|
XP_011512603.1:p.Gln1302His
|
|
XM_011514302.1:c.3750G>T
|
XP_011512604.1:p.Gln1250His
|
|
XM_011514299.2:c.4149G>T
|
XP_011512601.1:p.Gln1383His
|
|
XM_011514300.2:c.3969G>T
|
XP_011512602.1:p.Gln1323His
|
|
XM_011514302.2:c.3750G>T
|
XP_011512604.1:p.Gln1250His
|
|
XM_017010250.1:c.4863G>T
|
XP_016865739.1:p.Gln1621His
|
|
XM_017010251.2:c.3681G>T
|
XP_016865740.1:p.Gln1227His
|
|
NM_080680.3:c.4863G>T
MANE Select
|
NP_542411.2:p.Gln1621His
|
|
NM_080681.3:c.4605G>T
|
NP_542412.2:p.Gln1535His
|
|
NM_080679.3:c.4542G>T
|
NP_542410.2:p.Gln1514His
|
|