ENST00000315212.4:c.551G>C
MANE Select
|
ENSP00000313350.3:p.Arg184Thr
|
|
ENST00000654051.1:c.551G>C
|
ENSP00000499604.1:p.Arg184Thr
|
|
ENST00000658393.1:c.551G>C
|
ENSP00000499330.1:p.Arg184Thr
|
|
ENST00000315212.3:c.551G>C
|
ENSP00000313350.3:p.Arg184Thr
|
|
ENST00000436842.5:c.*657G>C
|
ENSP00000404926.1:n.*657G>C
|
|
NM_001286834.1:c.473G>C
|
NP_001273763.1:p.Arg158Thr
|
|
NM_001286837.1:c.200G>C
|
NP_001273766.1:p.Arg67Thr
|
|
NM_002936.4:c.551G>C
|
NP_002927.2:p.Arg184Thr
|
|
XR_244873.1:n.658G>C
|
|
|
XR_922665.1:n.658G>C
|
|
|
XR_922666.1:n.658G>C
|
|
|
XR_922667.1:n.658G>C
|
|
|
XR_922668.1:n.658G>C
|
|
|
XR_922669.1:n.658G>C
|
|
|
XR_922670.1:n.658G>C
|
|
|
XR_922671.1:n.658G>C
|
|
|
XR_922672.1:n.658G>C
|
|
|
XR_922673.1:n.658G>C
|
|
|
XR_922674.1:n.658G>C
|
|
|
NM_001286834.2:c.473G>C
|
NP_001273763.1:p.Arg158Thr
|
|
NM_001286837.2:c.200G>C
|
NP_001273766.1:p.Arg67Thr
|
|
NM_002936.5:c.551G>C
|
NP_002927.2:p.Arg184Thr
|
|
NR_148532.1:n.662G>C
|
|
|
NR_148533.1:n.662G>C
|
|
|
NR_148534.1:n.662G>C
|
|
|
NM_001286837.3:c.200G>C
|
NP_001273766.1:p.Arg67Thr
|
|
NR_148532.2:n.624G>C
|
|
|
NR_148533.2:n.624G>C
|
|
|
NR_148534.2:n.624G>C
|
|
|
NM_001286834.3:c.473G>C
|
NP_001273763.1:p.Arg158Thr
|
|
NM_001378271.1:c.551G>C
|
NP_001365200.1:p.Arg184Thr
|
|
NM_001378272.1:c.548G>C
|
NP_001365201.1:p.Arg183Thr
|
|
NM_001378273.1:c.536G>C
|
NP_001365202.1:p.Arg179Thr
|
|
NM_002936.6:c.551G>C
MANE Select
|
NP_002927.2:p.Arg184Thr
|
|
NR_165465.1:n.508G>C
|
|
|
NR_165466.1:n.593G>C
|
|
|
NR_165467.1:n.793G>C
|
|
|
NR_165468.1:n.596G>C
|
|
|