ENST00000683572.1:n.695C>T
|
|
|
ENST00000341947.7:c.4889C>T
MANE Select
|
ENSP00000339915.2:p.Ser1630Phe
|
|
ENST00000341947.6:c.4889C>T
|
ENSP00000339915.2:p.Ser1630Phe
|
|
ENST00000361917.5:c.4568C>T
|
ENSP00000355123.1:p.Ser1523Phe
|
|
ENST00000374708.8:c.4631C>T
|
ENSP00000363840.4:p.Ser1544Phe
|
|
ENST00000477772.1:n.679C>T
|
|
|
NM_080679.2:c.4568C>T
|
NP_542410.2:p.Ser1523Phe
|
|
NM_080680.2:c.4889C>T
|
NP_542411.2:p.Ser1630Phe
|
|
NM_080681.2:c.4631C>T
|
NP_542412.2:p.Ser1544Phe
|
|
XM_011514298.1:c.4043C>T
|
XP_011512600.1:p.Ser1348Phe
|
|
XM_011514299.1:c.4175C>T
|
XP_011512601.1:p.Ser1392Phe
|
|
XM_011514300.1:c.3995C>T
|
XP_011512602.1:p.Ser1332Phe
|
|
XM_011514301.1:c.3932C>T
|
XP_011512603.1:p.Ser1311Phe
|
|
XM_011514302.1:c.3776C>T
|
XP_011512604.1:p.Ser1259Phe
|
|
XM_011514299.2:c.4175C>T
|
XP_011512601.1:p.Ser1392Phe
|
|
XM_011514300.2:c.3995C>T
|
XP_011512602.1:p.Ser1332Phe
|
|
XM_011514302.2:c.3776C>T
|
XP_011512604.1:p.Ser1259Phe
|
|
XM_017010250.1:c.4889C>T
|
XP_016865739.1:p.Ser1630Phe
|
|
XM_017010251.2:c.3707C>T
|
XP_016865740.1:p.Ser1236Phe
|
|
NM_080680.3:c.4889C>T
MANE Select
|
NP_542411.2:p.Ser1630Phe
|
|
NM_080681.3:c.4631C>T
|
NP_542412.2:p.Ser1544Phe
|
|
NM_080679.3:c.4568C>T
|
NP_542410.2:p.Ser1523Phe
|
|