ENST00000683572.1:n.763T>C
|
|
|
ENST00000341947.7:c.4957T>C
MANE Select
|
ENSP00000339915.2:p.Tyr1653His
|
|
ENST00000341947.6:c.4957T>C
|
ENSP00000339915.2:p.Tyr1653His
|
|
ENST00000361917.5:c.4636T>C
|
ENSP00000355123.1:p.Tyr1546His
|
|
ENST00000374708.8:c.4699T>C
|
ENSP00000363840.4:p.Tyr1567His
|
|
ENST00000477772.1:n.747T>C
|
|
|
NM_080679.2:c.4636T>C
|
NP_542410.2:p.Tyr1546His
|
|
NM_080680.2:c.4957T>C
|
NP_542411.2:p.Tyr1653His
|
|
NM_080681.2:c.4699T>C
|
NP_542412.2:p.Tyr1567His
|
|
XM_011514298.1:c.4111T>C
|
XP_011512600.1:p.Tyr1371His
|
|
XM_011514299.1:c.4243T>C
|
XP_011512601.1:p.Tyr1415His
|
|
XM_011514300.1:c.4063T>C
|
XP_011512602.1:p.Tyr1355His
|
|
XM_011514301.1:c.4000T>C
|
XP_011512603.1:p.Tyr1334His
|
|
XM_011514302.1:c.3844T>C
|
XP_011512604.1:p.Tyr1282His
|
|
XM_011514299.2:c.4243T>C
|
XP_011512601.1:p.Tyr1415His
|
|
XM_011514300.2:c.4063T>C
|
XP_011512602.1:p.Tyr1355His
|
|
XM_011514302.2:c.3844T>C
|
XP_011512604.1:p.Tyr1282His
|
|
XM_017010250.1:c.4957T>C
|
XP_016865739.1:p.Tyr1653His
|
|
XM_017010251.2:c.3775T>C
|
XP_016865740.1:p.Tyr1259His
|
|
NM_080680.3:c.4957T>C
MANE Select
|
NP_542411.2:p.Tyr1653His
|
|
NM_080681.3:c.4699T>C
|
NP_542412.2:p.Tyr1567His
|
|
NM_080679.3:c.4636T>C
|
NP_542410.2:p.Tyr1546His
|
|