ENST00000317961.9:c.3685T>A
MANE Select
|
ENSP00000322408.4:p.Phe1229Ile
|
|
ENST00000317961.8:c.3685T>A
|
ENSP00000322408.4:p.Phe1229Ile
|
|
ENST00000382806.6:c.3514T>A
|
ENSP00000372256.2:p.Phe1172Ile
|
|
ENST00000415360.1:c.601T>A
|
ENSP00000389433.1:p.Phe201Ile
|
|
ENST00000440077.5:c.3562T>A
|
ENSP00000398543.1:p.Phe1188Ile
|
|
ENST00000469599.6:n.2283T>A
|
|
|
ENST00000492117.1:n.3577T>A
|
|
|
ENST00000541639.5:c.3778T>A
|
ENSP00000444293.1:p.Phe1260Ile
|
|
NM_001146705.1:c.3778T>A
|
NP_001140177.1:p.Phe1260Ile
|
|
NM_001146706.1:c.3514T>A
|
NP_001140178.1:p.Phe1172Ile
|
|
NM_004653.4:c.3685T>A
|
NP_004644.2:p.Phe1229Ile
|
|
XM_005262560.1:c.3550T>A
|
XP_005262617.1:p.Phe1184Ile
|
|
XM_005262561.1:c.3454T>A
|
XP_005262618.1:p.Phe1152Ile
|
|
XM_011531468.1:c.3607T>A
|
XP_011529770.1:p.Phe1203Ile
|
|
XR_244571.2:n.3973T>A
|
|
|
XR_430568.2:n.4307T>A
|
|
|
XM_005262560.3:c.3550T>A
|
XP_005262617.1:p.Phe1184Ile
|
|
XM_005262561.3:c.3454T>A
|
XP_005262618.1:p.Phe1152Ile
|
|
XM_011531468.3:c.3607T>A
|
XP_011529770.1:p.Phe1203Ile
|
|
XM_024452495.1:c.1675T>A
|
XP_024308263.1:p.Phe559Ile
|
|
XM_024452496.1:c.1441T>A
|
XP_024308264.1:p.Phe481Ile
|
|
XR_001756009.2:n.4423T>A
|
|
|
XR_001756010.2:n.4423T>A
|
|
|
XR_001756011.2:n.4288T>A
|
|
|
XR_001756012.2:n.4436T>A
|
|
|
XR_001756013.2:n.3754T>A
|
|
|
XR_002958832.1:n.3855T>A
|
|
|
XR_002958834.1:n.4079T>A
|
|
|
XR_002958835.1:n.3962T>A
|
|
|
XR_002958836.1:n.4645T>A
|
|
|
XR_002958837.1:n.4452T>A
|
|
|
XR_244571.4:n.3972T>A
|
|
|
XR_430568.4:n.4306T>A
|
|
|
NM_001146706.2:c.3514T>A
|
NP_001140178.1:p.Phe1172Ile
|
|
NM_004653.5:c.3685T>A
MANE Select
|
NP_004644.2:p.Phe1229Ile
|
|
NM_001146705.2:c.3778T>A
|
NP_001140177.1:p.Phe1260Ile
|
|