ENST00000527168.6:n.825G>T
|
|
|
ENST00000529110.2:c.810G>T
|
ENSP00000435349.2:p.Leu270=
|
|
ENST00000529957.6:n.784G>T
|
|
|
ENST00000683366.1:c.*458G>T
|
ENSP00000507283.1:n.*458G>T
|
|
ENST00000683887.1:c.774G>T
|
ENSP00000506886.1:p.Leu258=
|
|
ENST00000684100.1:n.720G>T
|
|
|
ENST00000684126.1:n.860G>T
|
|
|
ENST00000684688.1:n.1351G>T
|
|
|
ENST00000204679.9:c.726G>T
MANE Select
|
ENSP00000204679.4:p.Leu242=
|
|
ENST00000204679.8:c.726G>T
|
ENSP00000204679.4:p.Leu242=
|
|
ENST00000527076.1:n.1949G>T
|
|
|
ENST00000527168.5:n.893G>T
|
|
|
ENST00000529957.5:n.825G>T
|
|
|
NM_032520.4:c.726G>T
|
NP_115909.1:p.Leu242=
|
|
XM_017023782.1:c.774G>T
|
XP_016879271.1:p.Leu258=
|
|
XM_017023783.1:c.366G>T
|
XP_016879272.1:p.Leu122=
|
|
NM_032520.5:c.726G>T
MANE Select
|
NP_115909.1:p.Leu242=
|
|