ENST00000683572.1:n.754G>T
|
|
|
ENST00000341947.7:c.4948G>T
MANE Select
|
ENSP00000339915.2:p.Asp1650Tyr
|
|
ENST00000341947.6:c.4948G>T
|
ENSP00000339915.2:p.Asp1650Tyr
|
|
ENST00000361917.5:c.4627G>T
|
ENSP00000355123.1:p.Asp1543Tyr
|
|
ENST00000374708.8:c.4690G>T
|
ENSP00000363840.4:p.Asp1564Tyr
|
|
ENST00000477772.1:n.738G>T
|
|
|
NM_080679.2:c.4627G>T
|
NP_542410.2:p.Asp1543Tyr
|
|
NM_080680.2:c.4948G>T
|
NP_542411.2:p.Asp1650Tyr
|
|
NM_080681.2:c.4690G>T
|
NP_542412.2:p.Asp1564Tyr
|
|
XM_011514298.1:c.4102G>T
|
XP_011512600.1:p.Asp1368Tyr
|
|
XM_011514299.1:c.4234G>T
|
XP_011512601.1:p.Asp1412Tyr
|
|
XM_011514300.1:c.4054G>T
|
XP_011512602.1:p.Asp1352Tyr
|
|
XM_011514301.1:c.3991G>T
|
XP_011512603.1:p.Asp1331Tyr
|
|
XM_011514302.1:c.3835G>T
|
XP_011512604.1:p.Asp1279Tyr
|
|
XM_011514299.2:c.4234G>T
|
XP_011512601.1:p.Asp1412Tyr
|
|
XM_011514300.2:c.4054G>T
|
XP_011512602.1:p.Asp1352Tyr
|
|
XM_011514302.2:c.3835G>T
|
XP_011512604.1:p.Asp1279Tyr
|
|
XM_017010250.1:c.4948G>T
|
XP_016865739.1:p.Asp1650Tyr
|
|
XM_017010251.2:c.3766G>T
|
XP_016865740.1:p.Asp1256Tyr
|
|
NM_080680.3:c.4948G>T
MANE Select
|
NP_542411.2:p.Asp1650Tyr
|
|
NM_080681.3:c.4690G>T
|
NP_542412.2:p.Asp1564Tyr
|
|
NM_080679.3:c.4627G>T
|
NP_542410.2:p.Asp1543Tyr
|
|