ENST00000317961.9:c.4493C>G
MANE Select
|
ENSP00000322408.4:p.Thr1498Arg
|
|
ENST00000317961.8:c.4493C>G
|
ENSP00000322408.4:p.Thr1498Arg
|
|
ENST00000382806.6:c.4322C>G
|
ENSP00000372256.2:p.Thr1441Arg
|
|
ENST00000440077.5:c.4370C>G
|
ENSP00000398543.1:p.Thr1457Arg
|
|
ENST00000469599.6:n.3244C>G
|
|
|
ENST00000492117.1:n.4538C>G
|
|
|
ENST00000541639.5:c.4586C>G
|
ENSP00000444293.1:p.Thr1529Arg
|
|
NM_001146705.1:c.4586C>G
|
NP_001140177.1:p.Thr1529Arg
|
|
NM_001146706.1:c.4322C>G
|
NP_001140178.1:p.Thr1441Arg
|
|
NM_004653.4:c.4493C>G
|
NP_004644.2:p.Thr1498Arg
|
|
XM_005262560.1:c.4358C>G
|
XP_005262617.1:p.Thr1453Arg
|
|
XM_005262561.1:c.4262C>G
|
XP_005262618.1:p.Thr1421Arg
|
|
XM_011531468.1:c.4415C>G
|
XP_011529770.1:p.Thr1472Arg
|
|
XR_430568.2:n.5268C>G
|
|
|
XM_005262560.3:c.4358C>G
|
XP_005262617.1:p.Thr1453Arg
|
|
XM_005262561.3:c.4262C>G
|
XP_005262618.1:p.Thr1421Arg
|
|
XM_011531468.3:c.4415C>G
|
XP_011529770.1:p.Thr1472Arg
|
|
XM_024452495.1:c.2483C>G
|
XP_024308263.1:p.Thr828Arg
|
|
XM_024452496.1:c.2249C>G
|
XP_024308264.1:p.Thr750Arg
|
|
XR_001756009.2:n.5231C>G
|
|
|
XR_001756010.2:n.5199C>G
|
|
|
XR_001756011.2:n.5096C>G
|
|
|
XR_001756012.2:n.5244C>G
|
|
|
XR_001756013.2:n.4562C>G
|
|
|
XR_002958832.1:n.4816C>G
|
|
|
XR_002958834.1:n.4887C>G
|
|
|
XR_002958835.1:n.4770C>G
|
|
|
XR_002958836.1:n.5421C>G
|
|
|
XR_002958837.1:n.5228C>G
|
|
|
XR_244571.4:n.4748C>G
|
|
|
XR_430568.4:n.5267C>G
|
|
|
NM_001146706.2:c.4322C>G
|
NP_001140178.1:p.Thr1441Arg
|
|
NM_004653.5:c.4493C>G
MANE Select
|
NP_004644.2:p.Thr1498Arg
|
|
NM_001146705.2:c.4586C>G
|
NP_001140177.1:p.Thr1529Arg
|
|