ENST00000529510.6:n.885G>C
|
|
|
ENST00000697845.1:n.809G>C
|
|
|
ENST00000697846.1:n.885G>C
|
|
|
ENST00000697847.1:n.885G>C
|
|
|
ENST00000697848.1:n.885G>C
|
|
|
ENST00000697849.1:n.1924G>C
|
|
|
ENST00000697850.1:n.885G>C
|
|
|
ENST00000697851.1:n.2245G>C
|
|
|
ENST00000638186.1:n.959G>C
|
|
|
ENST00000638360.1:n.791G>C
|
|
|
ENST00000638925.1:n.892G>C
|
|
|
ENST00000650539.1:n.1061G>C
|
|
|
ENST00000330775.9:c.655G>C
|
ENSP00000476242.2:p.Glu219Gln
|
|
ENST00000357590.9:c.655G>C
|
ENSP00000476176.2:p.Glu219Gln
|
|
ENST00000524428.5:n.977G>C
|
|
|
ENST00000525039.5:n.1079G>C
|
|
|
ENST00000525102.5:n.1413G>C
|
|
|
ENST00000525372.5:n.656G>C
|
|
|
ENST00000526275.5:n.1437G>C
|
|
|
ENST00000526626.6:n.618G>C
|
|
|
ENST00000527992.5:n.883G>C
|
|
|
ENST00000529510.5:n.429G>C
|
|
|
ENST00000530407.5:n.805G>C
|
|
|
ENST00000532085.1:n.3266G>C
|
|
|
ENST00000532888.6:n.951G>C
|
|
|
ENST00000538950.5:c.436G>C
|
ENSP00000475991.2:p.Glu146Gln
|
|
ENST00000545985.5:c.655G>C
|
ENSP00000475241.2:p.Glu219Gln
|
|
NM_001164277.1:c.655G>C , LRG_187t1:c.655G>C
|
NP_001157749.1:p.Glu219Gln
|
|
NM_001164278.1:c.655G>C
|
NP_001157750.1:p.Glu219Gln
|
|
NM_001164279.1:c.436G>C
|
NP_001157751.1:p.Glu146Gln
|
|
NM_001164280.1:c.655G>C
|
NP_001157752.1:p.Glu219Gln
|
|
NM_001467.5:c.655G>C
|
NP_001458.1:p.Glu219Gln
|
|
NM_001164278.2:c.655G>C
|
NP_001157750.1:p.Glu219Gln
|
|
NM_001164279.2:c.436G>C
|
NP_001157751.1:p.Glu146Gln
|
|
NM_001164280.2:c.655G>C
|
NP_001157752.1:p.Glu219Gln
|
|
NM_001467.6:c.655G>C
|
NP_001458.1:p.Glu219Gln
|
|
NM_001164277.2:c.655G>C
MANE Select
|
NP_001157749.1:p.Glu219Gln
|
|