ENST00000683572.1:n.568G>A
|
|
|
ENST00000341947.7:c.4762G>A
MANE Select
|
ENSP00000339915.2:p.Val1588Ile
|
|
ENST00000341947.6:c.4762G>A
|
ENSP00000339915.2:p.Val1588Ile
|
|
ENST00000361917.5:c.4441G>A
|
ENSP00000355123.1:p.Val1481Ile
|
|
ENST00000374708.8:c.4504G>A
|
ENSP00000363840.4:p.Val1502Ile
|
|
ENST00000477772.1:n.552G>A
|
|
|
NM_080679.2:c.4441G>A
|
NP_542410.2:p.Val1481Ile
|
|
NM_080680.2:c.4762G>A
|
NP_542411.2:p.Val1588Ile
|
|
NM_080681.2:c.4504G>A
|
NP_542412.2:p.Val1502Ile
|
|
XM_011514298.1:c.3916G>A
|
XP_011512600.1:p.Val1306Ile
|
|
XM_011514299.1:c.4048G>A
|
XP_011512601.1:p.Val1350Ile
|
|
XM_011514300.1:c.3868G>A
|
XP_011512602.1:p.Val1290Ile
|
|
XM_011514301.1:c.3805G>A
|
XP_011512603.1:p.Val1269Ile
|
|
XM_011514302.1:c.3649G>A
|
XP_011512604.1:p.Val1217Ile
|
|
XM_011514299.2:c.4048G>A
|
XP_011512601.1:p.Val1350Ile
|
|
XM_011514300.2:c.3868G>A
|
XP_011512602.1:p.Val1290Ile
|
|
XM_011514302.2:c.3649G>A
|
XP_011512604.1:p.Val1217Ile
|
|
XM_017010250.1:c.4762G>A
|
XP_016865739.1:p.Val1588Ile
|
|
XM_017010251.2:c.3580G>A
|
XP_016865740.1:p.Val1194Ile
|
|
NM_080680.3:c.4762G>A
MANE Select
|
NP_542411.2:p.Val1588Ile
|
|
NM_080681.3:c.4504G>A
|
NP_542412.2:p.Val1502Ile
|
|
NM_080679.3:c.4441G>A
|
NP_542410.2:p.Val1481Ile
|
|