ENST00000317961.9:c.3461C>A
MANE Select
|
ENSP00000322408.4:p.Thr1154Asn
|
|
ENST00000317961.8:c.3461C>A
|
ENSP00000322408.4:p.Thr1154Asn
|
|
ENST00000382806.6:c.3290C>A
|
ENSP00000372256.2:p.Thr1097Asn
|
|
ENST00000415360.1:c.377C>A
|
ENSP00000389433.1:p.Thr126Asn
|
|
ENST00000440077.5:c.3338C>A
|
ENSP00000398543.1:p.Thr1113Asn
|
|
ENST00000469599.6:n.2059C>A
|
|
|
ENST00000492117.1:n.3353C>A
|
|
|
ENST00000541639.5:c.3554C>A
|
ENSP00000444293.1:p.Thr1185Asn
|
|
NM_001146705.1:c.3554C>A
|
NP_001140177.1:p.Thr1185Asn
|
|
NM_001146706.1:c.3290C>A
|
NP_001140178.1:p.Thr1097Asn
|
|
NM_004653.4:c.3461C>A
|
NP_004644.2:p.Thr1154Asn
|
|
XM_005262560.1:c.3326C>A
|
XP_005262617.1:p.Thr1109Asn
|
|
XM_005262561.1:c.3230C>A
|
XP_005262618.1:p.Thr1077Asn
|
|
XM_011531468.1:c.3383C>A
|
XP_011529770.1:p.Thr1128Asn
|
|
XR_244571.2:n.3749C>A
|
|
|
XR_430568.2:n.4083C>A
|
|
|
XM_005262560.3:c.3326C>A
|
XP_005262617.1:p.Thr1109Asn
|
|
XM_005262561.3:c.3230C>A
|
XP_005262618.1:p.Thr1077Asn
|
|
XM_011531468.3:c.3383C>A
|
XP_011529770.1:p.Thr1128Asn
|
|
XM_024452495.1:c.1451C>A
|
XP_024308263.1:p.Thr484Asn
|
|
XM_024452496.1:c.1217C>A
|
XP_024308264.1:p.Thr406Asn
|
|
XR_001756009.2:n.4199C>A
|
|
|
XR_001756010.2:n.4199C>A
|
|
|
XR_001756011.2:n.4064C>A
|
|
|
XR_001756012.2:n.4212C>A
|
|
|
XR_001756013.2:n.3530C>A
|
|
|
XR_002958832.1:n.3631C>A
|
|
|
XR_002958834.1:n.3855C>A
|
|
|
XR_002958835.1:n.3738C>A
|
|
|
XR_002958836.1:n.4421C>A
|
|
|
XR_002958837.1:n.4228C>A
|
|
|
XR_244571.4:n.3748C>A
|
|
|
XR_430568.4:n.4082C>A
|
|
|
NM_001146706.2:c.3290C>A
|
NP_001140178.1:p.Thr1097Asn
|
|
NM_004653.5:c.3461C>A
MANE Select
|
NP_004644.2:p.Thr1154Asn
|
|
NM_001146705.2:c.3554C>A
|
NP_001140177.1:p.Thr1185Asn
|
|