ENST00000317961.9:c.3565T>C
MANE Select
|
ENSP00000322408.4:p.Cys1189Arg
|
|
ENST00000317961.8:c.3565T>C
|
ENSP00000322408.4:p.Cys1189Arg
|
|
ENST00000382806.6:c.3394T>C
|
ENSP00000372256.2:p.Cys1132Arg
|
|
ENST00000415360.1:c.481T>C
|
ENSP00000389433.1:p.Cys161Arg
|
|
ENST00000440077.5:c.3442T>C
|
ENSP00000398543.1:p.Cys1148Arg
|
|
ENST00000469599.6:n.2163T>C
|
|
|
ENST00000492117.1:n.3457T>C
|
|
|
ENST00000541639.5:c.3658T>C
|
ENSP00000444293.1:p.Cys1220Arg
|
|
NM_001146705.1:c.3658T>C
|
NP_001140177.1:p.Cys1220Arg
|
|
NM_001146706.1:c.3394T>C
|
NP_001140178.1:p.Cys1132Arg
|
|
NM_004653.4:c.3565T>C
|
NP_004644.2:p.Cys1189Arg
|
|
XM_005262560.1:c.3430T>C
|
XP_005262617.1:p.Cys1144Arg
|
|
XM_005262561.1:c.3334T>C
|
XP_005262618.1:p.Cys1112Arg
|
|
XM_011531468.1:c.3487T>C
|
XP_011529770.1:p.Cys1163Arg
|
|
XR_244571.2:n.3853T>C
|
|
|
XR_430568.2:n.4187T>C
|
|
|
XM_005262560.3:c.3430T>C
|
XP_005262617.1:p.Cys1144Arg
|
|
XM_005262561.3:c.3334T>C
|
XP_005262618.1:p.Cys1112Arg
|
|
XM_011531468.3:c.3487T>C
|
XP_011529770.1:p.Cys1163Arg
|
|
XM_024452495.1:c.1555T>C
|
XP_024308263.1:p.Cys519Arg
|
|
XM_024452496.1:c.1321T>C
|
XP_024308264.1:p.Cys441Arg
|
|
XR_001756009.2:n.4303T>C
|
|
|
XR_001756010.2:n.4303T>C
|
|
|
XR_001756011.2:n.4168T>C
|
|
|
XR_001756012.2:n.4316T>C
|
|
|
XR_001756013.2:n.3634T>C
|
|
|
XR_002958832.1:n.3735T>C
|
|
|
XR_002958834.1:n.3959T>C
|
|
|
XR_002958835.1:n.3842T>C
|
|
|
XR_002958836.1:n.4525T>C
|
|
|
XR_002958837.1:n.4332T>C
|
|
|
XR_244571.4:n.3852T>C
|
|
|
XR_430568.4:n.4186T>C
|
|
|
NM_001146706.2:c.3394T>C
|
NP_001140178.1:p.Cys1132Arg
|
|
NM_004653.5:c.3565T>C
MANE Select
|
NP_004644.2:p.Cys1189Arg
|
|
NM_001146705.2:c.3658T>C
|
NP_001140177.1:p.Cys1220Arg
|
|