ENST00000683572.1:n.758T>C
|
|
|
ENST00000341947.7:c.4952T>C
MANE Select
|
ENSP00000339915.2:p.Val1651Ala
|
|
ENST00000341947.6:c.4952T>C
|
ENSP00000339915.2:p.Val1651Ala
|
|
ENST00000361917.5:c.4631T>C
|
ENSP00000355123.1:p.Val1544Ala
|
|
ENST00000374708.8:c.4694T>C
|
ENSP00000363840.4:p.Val1565Ala
|
|
ENST00000477772.1:n.742T>C
|
|
|
NM_080679.2:c.4631T>C
|
NP_542410.2:p.Val1544Ala
|
|
NM_080680.2:c.4952T>C
|
NP_542411.2:p.Val1651Ala
|
|
NM_080681.2:c.4694T>C
|
NP_542412.2:p.Val1565Ala
|
|
XM_011514298.1:c.4106T>C
|
XP_011512600.1:p.Val1369Ala
|
|
XM_011514299.1:c.4238T>C
|
XP_011512601.1:p.Val1413Ala
|
|
XM_011514300.1:c.4058T>C
|
XP_011512602.1:p.Val1353Ala
|
|
XM_011514301.1:c.3995T>C
|
XP_011512603.1:p.Val1332Ala
|
|
XM_011514302.1:c.3839T>C
|
XP_011512604.1:p.Val1280Ala
|
|
XM_011514299.2:c.4238T>C
|
XP_011512601.1:p.Val1413Ala
|
|
XM_011514300.2:c.4058T>C
|
XP_011512602.1:p.Val1353Ala
|
|
XM_011514302.2:c.3839T>C
|
XP_011512604.1:p.Val1280Ala
|
|
XM_017010250.1:c.4952T>C
|
XP_016865739.1:p.Val1651Ala
|
|
XM_017010251.2:c.3770T>C
|
XP_016865740.1:p.Val1257Ala
|
|
NM_080680.3:c.4952T>C
MANE Select
|
NP_542411.2:p.Val1651Ala
|
|
NM_080681.3:c.4694T>C
|
NP_542412.2:p.Val1565Ala
|
|
NM_080679.3:c.4631T>C
|
NP_542410.2:p.Val1544Ala
|
|