ENST00000683572.1:n.619T>G
|
|
|
ENST00000341947.7:c.4813T>G
MANE Select
|
ENSP00000339915.2:p.Phe1605Val
|
|
ENST00000341947.6:c.4813T>G
|
ENSP00000339915.2:p.Phe1605Val
|
|
ENST00000361917.5:c.4492T>G
|
ENSP00000355123.1:p.Phe1498Val
|
|
ENST00000374708.8:c.4555T>G
|
ENSP00000363840.4:p.Phe1519Val
|
|
ENST00000477772.1:n.603T>G
|
|
|
NM_080679.2:c.4492T>G
|
NP_542410.2:p.Phe1498Val
|
|
NM_080680.2:c.4813T>G
|
NP_542411.2:p.Phe1605Val
|
|
NM_080681.2:c.4555T>G
|
NP_542412.2:p.Phe1519Val
|
|
XM_011514298.1:c.3967T>G
|
XP_011512600.1:p.Phe1323Val
|
|
XM_011514299.1:c.4099T>G
|
XP_011512601.1:p.Phe1367Val
|
|
XM_011514300.1:c.3919T>G
|
XP_011512602.1:p.Phe1307Val
|
|
XM_011514301.1:c.3856T>G
|
XP_011512603.1:p.Phe1286Val
|
|
XM_011514302.1:c.3700T>G
|
XP_011512604.1:p.Phe1234Val
|
|
XM_011514299.2:c.4099T>G
|
XP_011512601.1:p.Phe1367Val
|
|
XM_011514300.2:c.3919T>G
|
XP_011512602.1:p.Phe1307Val
|
|
XM_011514302.2:c.3700T>G
|
XP_011512604.1:p.Phe1234Val
|
|
XM_017010250.1:c.4813T>G
|
XP_016865739.1:p.Phe1605Val
|
|
XM_017010251.2:c.3631T>G
|
XP_016865740.1:p.Phe1211Val
|
|
NM_080680.3:c.4813T>G
MANE Select
|
NP_542411.2:p.Phe1605Val
|
|
NM_080681.3:c.4555T>G
|
NP_542412.2:p.Phe1519Val
|
|
NM_080679.3:c.4492T>G
|
NP_542410.2:p.Phe1498Val
|
|