|
ENST00000556892.6:c.164G>T
|
ENSP00000452206.2:p.Gly55Val
|
|
|
ENST00000556979.6:c.*836G>T
|
ENSP00000452378.1:n.*836G>T
|
|
|
ENST00000358664.9:c.383G>T
MANE Select
|
ENSP00000351490.4:p.Gly128Val
|
|
|
ENST00000651648.1:c.145-6207G>T
|
ENSP00000498863.1:n.145-6207G>T
|
|
|
ENST00000284165.10:c.*1227G>T
|
ENSP00000284165.6:n.*1227G>T
|
|
|
ENST00000341653.6:c.171+17132G>T
|
ENSP00000342482.2:n.171+17132G>T
|
|
|
ENST00000358402.8:c.356G>T
|
ENSP00000351175.4:p.Gly119Val
|
|
|
ENST00000358664.8:c.383G>T
|
ENSP00000351490.4:p.Gly128Val
|
|
|
ENST00000394606.6:c.*156G>T
|
ENSP00000378104.2:n.*156G>T
|
|
|
ENST00000553928.5:c.*172G>T
|
ENSP00000451907.1:n.*172G>T
|
|
|
ENST00000555419.5:c.275G>T
|
ENSP00000452405.1:p.Gly92Val
|
|
|
ENST00000555932.5:c.124G>T
|
ENSP00000450763.1:p.Ala42Ser
|
|
|
ENST00000557277.5:c.194G>T
|
ENSP00000450955.1:p.Gly65Val
|
|
|
ENST00000618858.4:c.*172G>T
|
ENSP00000480127.1:n.*172G>T
|
|
|
NM_001271069.1:c.144+17132G>T
|
NP_001257998.1:n.144+17132G>T
|
|
|
NM_002382.4:c.383G>T
|
NP_002373.3:p.Gly128Val
|
|
|
NM_145112.2:c.356G>T
|
NP_660087.1:p.Gly119Val
|
|
|
NM_145113.2:c.*172G>T
|
NP_660088.1:n.*172G>T
|
|
|
NM_197957.3:c.171+17132G>T
|
NP_932061.1:n.171+17132G>T
|
|
|
NR_073137.1:n.507G>T
|
|
|
|
XR_429315.2:n.670G>T
|
|
|
|
XR_943451.1:n.767G>T
|
|
|
|
NM_001320415.1:c.194G>T
|
NP_001307344.1:p.Gly65Val
|
|
|
XM_017021312.2:c.194G>T
|
XP_016876801.1:p.Gly65Val
|
|
|
XM_017021313.1:c.194G>T
|
XP_016876802.1:p.Gly65Val
|
|
|
XR_001750326.2:n.728G>T
|
|
|
|
XR_001750327.2:n.647G>T
|
|
|
|
XR_002957553.1:n.1161G>T
|
|
|
|
XR_943450.3:n.751G>T
|
|
|
|
XR_943451.3:n.767G>T
|
|
|
|
XR_943452.3:n.712G>T
|
|
|
|
NM_001320415.2:c.194G>T
|
NP_001307344.1:p.Gly65Val
|
|
|
NM_002382.5:c.383G>T
MANE Select
|
NP_002373.3:p.Gly128Val
|
|
|
NM_145112.3:c.356G>T
|
NP_660087.1:p.Gly119Val
|
|
|
NM_145113.3:c.*172G>T
|
NP_660088.1:n.*172G>T
|
|
|
NM_001271069.2:c.144+17132G>T
|
NP_001257998.1:n.144+17132G>T
|
|
|
NM_197957.4:c.171+17132G>T
|
NP_932061.1:n.171+17132G>T
|
|
