ENST00000683572.1:n.620T>C
|
|
|
ENST00000341947.7:c.4814T>C
MANE Select
|
ENSP00000339915.2:p.Phe1605Ser
|
|
ENST00000341947.6:c.4814T>C
|
ENSP00000339915.2:p.Phe1605Ser
|
|
ENST00000361917.5:c.4493T>C
|
ENSP00000355123.1:p.Phe1498Ser
|
|
ENST00000374708.8:c.4556T>C
|
ENSP00000363840.4:p.Phe1519Ser
|
|
ENST00000477772.1:n.604T>C
|
|
|
NM_080679.2:c.4493T>C
|
NP_542410.2:p.Phe1498Ser
|
|
NM_080680.2:c.4814T>C
|
NP_542411.2:p.Phe1605Ser
|
|
NM_080681.2:c.4556T>C
|
NP_542412.2:p.Phe1519Ser
|
|
XM_011514298.1:c.3968T>C
|
XP_011512600.1:p.Phe1323Ser
|
|
XM_011514299.1:c.4100T>C
|
XP_011512601.1:p.Phe1367Ser
|
|
XM_011514300.1:c.3920T>C
|
XP_011512602.1:p.Phe1307Ser
|
|
XM_011514301.1:c.3857T>C
|
XP_011512603.1:p.Phe1286Ser
|
|
XM_011514302.1:c.3701T>C
|
XP_011512604.1:p.Phe1234Ser
|
|
XM_011514299.2:c.4100T>C
|
XP_011512601.1:p.Phe1367Ser
|
|
XM_011514300.2:c.3920T>C
|
XP_011512602.1:p.Phe1307Ser
|
|
XM_011514302.2:c.3701T>C
|
XP_011512604.1:p.Phe1234Ser
|
|
XM_017010250.1:c.4814T>C
|
XP_016865739.1:p.Phe1605Ser
|
|
XM_017010251.2:c.3632T>C
|
XP_016865740.1:p.Phe1211Ser
|
|
NM_080680.3:c.4814T>C
MANE Select
|
NP_542411.2:p.Phe1605Ser
|
|
NM_080681.3:c.4556T>C
|
NP_542412.2:p.Phe1519Ser
|
|
NM_080679.3:c.4493T>C
|
NP_542410.2:p.Phe1498Ser
|
|