ENST00000683572.1:n.609T>A
|
|
|
ENST00000341947.7:c.4803T>A
MANE Select
|
ENSP00000339915.2:p.Val1601=
|
|
ENST00000341947.6:c.4803T>A
|
ENSP00000339915.2:p.Val1601=
|
|
ENST00000361917.5:c.4482T>A
|
ENSP00000355123.1:p.Val1494=
|
|
ENST00000374708.8:c.4545T>A
|
ENSP00000363840.4:p.Val1515=
|
|
ENST00000477772.1:n.593T>A
|
|
|
NM_080679.2:c.4482T>A
|
NP_542410.2:p.Val1494=
|
|
NM_080680.2:c.4803T>A
|
NP_542411.2:p.Val1601=
|
|
NM_080681.2:c.4545T>A
|
NP_542412.2:p.Val1515=
|
|
XM_011514298.1:c.3957T>A
|
XP_011512600.1:p.Val1319=
|
|
XM_011514299.1:c.4089T>A
|
XP_011512601.1:p.Val1363=
|
|
XM_011514300.1:c.3909T>A
|
XP_011512602.1:p.Val1303=
|
|
XM_011514301.1:c.3846T>A
|
XP_011512603.1:p.Val1282=
|
|
XM_011514302.1:c.3690T>A
|
XP_011512604.1:p.Val1230=
|
|
XM_011514299.2:c.4089T>A
|
XP_011512601.1:p.Val1363=
|
|
XM_011514300.2:c.3909T>A
|
XP_011512602.1:p.Val1303=
|
|
XM_011514302.2:c.3690T>A
|
XP_011512604.1:p.Val1230=
|
|
XM_017010250.1:c.4803T>A
|
XP_016865739.1:p.Val1601=
|
|
XM_017010251.2:c.3621T>A
|
XP_016865740.1:p.Val1207=
|
|
NM_080680.3:c.4803T>A
MANE Select
|
NP_542411.2:p.Val1601=
|
|
NM_080681.3:c.4545T>A
|
NP_542412.2:p.Val1515=
|
|
NM_080679.3:c.4482T>A
|
NP_542410.2:p.Val1494=
|
|