ENST00000527168.6:n.542T>G
|
|
|
ENST00000529110.2:c.527T>G
|
ENSP00000435349.2:p.Leu176Arg
|
|
ENST00000529957.6:n.501T>G
|
|
|
ENST00000683366.1:c.*175T>G
|
ENSP00000507283.1:n.*175T>G
|
|
ENST00000683887.1:c.491T>G
|
ENSP00000506886.1:p.Leu164Arg
|
|
ENST00000684100.1:n.437T>G
|
|
|
ENST00000684126.1:n.501T>G
|
|
|
ENST00000684688.1:n.1068T>G
|
|
|
ENST00000204679.9:c.443T>G
MANE Select
|
ENSP00000204679.4:p.Leu148Arg
|
|
ENST00000204679.8:c.443T>G
|
ENSP00000204679.4:p.Leu148Arg
|
|
ENST00000527076.1:n.1459T>G
|
|
|
ENST00000527168.5:n.479T>G
|
|
|
ENST00000529110.1:c.510T>G
|
|
|
ENST00000529957.5:n.542T>G
|
|
|
NM_032520.4:c.443T>G
|
NP_115909.1:p.Leu148Arg
|
|
XM_017023782.1:c.491T>G
|
XP_016879271.1:p.Leu164Arg
|
|
XM_017023783.1:c.83T>G
|
XP_016879272.1:p.Leu28Arg
|
|
NM_032520.5:c.443T>G
MANE Select
|
NP_115909.1:p.Leu148Arg
|
|