ENST00000683572.1:n.582G>C
|
|
|
ENST00000341947.7:c.4776G>C
MANE Select
|
ENSP00000339915.2:p.Gln1592His
|
|
ENST00000341947.6:c.4776G>C
|
ENSP00000339915.2:p.Gln1592His
|
|
ENST00000361917.5:c.4455G>C
|
ENSP00000355123.1:p.Gln1485His
|
|
ENST00000374708.8:c.4518G>C
|
ENSP00000363840.4:p.Gln1506His
|
|
ENST00000477772.1:n.566G>C
|
|
|
NM_080679.2:c.4455G>C
|
NP_542410.2:p.Gln1485His
|
|
NM_080680.2:c.4776G>C
|
NP_542411.2:p.Gln1592His
|
|
NM_080681.2:c.4518G>C
|
NP_542412.2:p.Gln1506His
|
|
XM_011514298.1:c.3930G>C
|
XP_011512600.1:p.Gln1310His
|
|
XM_011514299.1:c.4062G>C
|
XP_011512601.1:p.Gln1354His
|
|
XM_011514300.1:c.3882G>C
|
XP_011512602.1:p.Gln1294His
|
|
XM_011514301.1:c.3819G>C
|
XP_011512603.1:p.Gln1273His
|
|
XM_011514302.1:c.3663G>C
|
XP_011512604.1:p.Gln1221His
|
|
XM_011514299.2:c.4062G>C
|
XP_011512601.1:p.Gln1354His
|
|
XM_011514300.2:c.3882G>C
|
XP_011512602.1:p.Gln1294His
|
|
XM_011514302.2:c.3663G>C
|
XP_011512604.1:p.Gln1221His
|
|
XM_017010250.1:c.4776G>C
|
XP_016865739.1:p.Gln1592His
|
|
XM_017010251.2:c.3594G>C
|
XP_016865740.1:p.Gln1198His
|
|
NM_080680.3:c.4776G>C
MANE Select
|
NP_542411.2:p.Gln1592His
|
|
NM_080681.3:c.4518G>C
|
NP_542412.2:p.Gln1506His
|
|
NM_080679.3:c.4455G>C
|
NP_542410.2:p.Gln1485His
|
|