|
ENST00000556892.6:c.224A>T
|
ENSP00000452206.2:p.Glu75Val
|
|
|
ENST00000556979.6:c.*896A>T
|
ENSP00000452378.1:n.*896A>T
|
|
|
ENST00000358664.9:c.443A>T
MANE Select
|
ENSP00000351490.4:p.Glu148Val
|
|
|
ENST00000651648.1:c.145-6147A>T
|
ENSP00000498863.1:n.145-6147A>T
|
|
|
ENST00000284165.10:c.*1287A>T
|
ENSP00000284165.6:n.*1287A>T
|
|
|
ENST00000341653.6:c.171+17192A>T
|
ENSP00000342482.2:n.171+17192A>T
|
|
|
ENST00000358402.8:c.416A>T
|
ENSP00000351175.4:p.Glu139Val
|
|
|
ENST00000358664.8:c.443A>T
|
ENSP00000351490.4:p.Glu148Val
|
|
|
ENST00000394606.6:c.*216A>T
|
ENSP00000378104.2:n.*216A>T
|
|
|
ENST00000553928.5:c.*232A>T
|
ENSP00000451907.1:n.*232A>T
|
|
|
ENST00000555419.5:c.335A>T
|
ENSP00000452405.1:p.Glu112Val
|
|
|
ENST00000555932.5:c.184A>T
|
ENSP00000450763.1:p.Ser62Cys
|
|
|
ENST00000557277.5:c.254A>T
|
ENSP00000450955.1:p.Glu85Val
|
|
|
ENST00000618858.4:c.*232A>T
|
ENSP00000480127.1:n.*232A>T
|
|
|
NM_001271069.1:c.144+17192A>T
|
NP_001257998.1:n.144+17192A>T
|
|
|
NM_002382.4:c.443A>T
|
NP_002373.3:p.Glu148Val
|
|
|
NM_145112.2:c.416A>T
|
NP_660087.1:p.Glu139Val
|
|
|
NM_145113.2:c.*232A>T
|
NP_660088.1:n.*232A>T
|
|
|
NM_197957.3:c.171+17192A>T
|
NP_932061.1:n.171+17192A>T
|
|
|
NR_073137.1:n.567A>T
|
|
|
|
XR_429315.2:n.730A>T
|
|
|
|
NM_001320415.1:c.254A>T
|
NP_001307344.1:p.Glu85Val
|
|
|
XM_017021312.2:c.254A>T
|
XP_016876801.1:p.Glu85Val
|
|
|
XM_017021313.1:c.254A>T
|
XP_016876802.1:p.Glu85Val
|
|
|
XR_001750326.2:n.788A>T
|
|
|
|
XR_001750327.2:n.707A>T
|
|
|
|
XR_002957553.1:n.1221A>T
|
|
|
|
XR_943450.3:n.811A>T
|
|
|
|
XR_943451.3:n.827A>T
|
|
|
|
XR_943452.3:n.772A>T
|
|
|
|
NM_001320415.2:c.254A>T
|
NP_001307344.1:p.Glu85Val
|
|
|
NM_002382.5:c.443A>T
MANE Select
|
NP_002373.3:p.Glu148Val
|
|
|
NM_145112.3:c.416A>T
|
NP_660087.1:p.Glu139Val
|
|
|
NM_145113.3:c.*232A>T
|
NP_660088.1:n.*232A>T
|
|
|
NM_001271069.2:c.144+17192A>T
|
NP_001257998.1:n.144+17192A>T
|
|
|
NM_197957.4:c.171+17192A>T
|
NP_932061.1:n.171+17192A>T
|
|
