ENST00000317961.9:c.3707G>C
MANE Select
|
ENSP00000322408.4:p.Arg1236Pro
|
|
ENST00000317961.8:c.3707G>C
|
ENSP00000322408.4:p.Arg1236Pro
|
|
ENST00000382806.6:c.3536G>C
|
ENSP00000372256.2:p.Arg1179Pro
|
|
ENST00000415360.1:c.623G>C
|
ENSP00000389433.1:p.Arg208Pro
|
|
ENST00000440077.5:c.3584G>C
|
ENSP00000398543.1:p.Arg1195Pro
|
|
ENST00000469599.6:n.2305G>C
|
|
|
ENST00000492117.1:n.3599G>C
|
|
|
ENST00000541639.5:c.3800G>C
|
ENSP00000444293.1:p.Arg1267Pro
|
|
NM_001146705.1:c.3800G>C
|
NP_001140177.1:p.Arg1267Pro
|
|
NM_001146706.1:c.3536G>C
|
NP_001140178.1:p.Arg1179Pro
|
|
NM_004653.4:c.3707G>C
|
NP_004644.2:p.Arg1236Pro
|
|
XM_005262560.1:c.3572G>C
|
XP_005262617.1:p.Arg1191Pro
|
|
XM_005262561.1:c.3476G>C
|
XP_005262618.1:p.Arg1159Pro
|
|
XM_011531468.1:c.3629G>C
|
XP_011529770.1:p.Arg1210Pro
|
|
XR_244571.2:n.3995G>C
|
|
|
XR_430568.2:n.4329G>C
|
|
|
XM_005262560.3:c.3572G>C
|
XP_005262617.1:p.Arg1191Pro
|
|
XM_005262561.3:c.3476G>C
|
XP_005262618.1:p.Arg1159Pro
|
|
XM_011531468.3:c.3629G>C
|
XP_011529770.1:p.Arg1210Pro
|
|
XM_024452495.1:c.1697G>C
|
XP_024308263.1:p.Arg566Pro
|
|
XM_024452496.1:c.1463G>C
|
XP_024308264.1:p.Arg488Pro
|
|
XR_001756009.2:n.4445G>C
|
|
|
XR_001756010.2:n.4445G>C
|
|
|
XR_001756011.2:n.4310G>C
|
|
|
XR_001756012.2:n.4458G>C
|
|
|
XR_001756013.2:n.3776G>C
|
|
|
XR_002958832.1:n.3877G>C
|
|
|
XR_002958834.1:n.4101G>C
|
|
|
XR_002958835.1:n.3984G>C
|
|
|
XR_002958836.1:n.4667G>C
|
|
|
XR_002958837.1:n.4474G>C
|
|
|
XR_244571.4:n.3994G>C
|
|
|
XR_430568.4:n.4328G>C
|
|
|
NM_001146706.2:c.3536G>C
|
NP_001140178.1:p.Arg1179Pro
|
|
NM_004653.5:c.3707G>C
MANE Select
|
NP_004644.2:p.Arg1236Pro
|
|
NM_001146705.2:c.3800G>C
|
NP_001140177.1:p.Arg1267Pro
|
|