ENST00000683572.1:n.620T>A
|
|
|
ENST00000341947.7:c.4814T>A
MANE Select
|
ENSP00000339915.2:p.Phe1605Tyr
|
|
ENST00000341947.6:c.4814T>A
|
ENSP00000339915.2:p.Phe1605Tyr
|
|
ENST00000361917.5:c.4493T>A
|
ENSP00000355123.1:p.Phe1498Tyr
|
|
ENST00000374708.8:c.4556T>A
|
ENSP00000363840.4:p.Phe1519Tyr
|
|
ENST00000477772.1:n.604T>A
|
|
|
NM_080679.2:c.4493T>A
|
NP_542410.2:p.Phe1498Tyr
|
|
NM_080680.2:c.4814T>A
|
NP_542411.2:p.Phe1605Tyr
|
|
NM_080681.2:c.4556T>A
|
NP_542412.2:p.Phe1519Tyr
|
|
XM_011514298.1:c.3968T>A
|
XP_011512600.1:p.Phe1323Tyr
|
|
XM_011514299.1:c.4100T>A
|
XP_011512601.1:p.Phe1367Tyr
|
|
XM_011514300.1:c.3920T>A
|
XP_011512602.1:p.Phe1307Tyr
|
|
XM_011514301.1:c.3857T>A
|
XP_011512603.1:p.Phe1286Tyr
|
|
XM_011514302.1:c.3701T>A
|
XP_011512604.1:p.Phe1234Tyr
|
|
XM_011514299.2:c.4100T>A
|
XP_011512601.1:p.Phe1367Tyr
|
|
XM_011514300.2:c.3920T>A
|
XP_011512602.1:p.Phe1307Tyr
|
|
XM_011514302.2:c.3701T>A
|
XP_011512604.1:p.Phe1234Tyr
|
|
XM_017010250.1:c.4814T>A
|
XP_016865739.1:p.Phe1605Tyr
|
|
XM_017010251.2:c.3632T>A
|
XP_016865740.1:p.Phe1211Tyr
|
|
NM_080680.3:c.4814T>A
MANE Select
|
NP_542411.2:p.Phe1605Tyr
|
|
NM_080681.3:c.4556T>A
|
NP_542412.2:p.Phe1519Tyr
|
|
NM_080679.3:c.4493T>A
|
NP_542410.2:p.Phe1498Tyr
|
|