ENST00000682275.1:c.1077G>T
|
ENSP00000507852.1:p.Leu359=
|
|
ENST00000683395.1:c.1018G>T
|
|
|
ENST00000684087.1:c.1041G>T
|
ENSP00000506978.1:p.Leu347=
|
|
ENST00000506362.2:c.792G>T
|
ENSP00000424103.2:p.Leu264=
|
|
ENST00000673642.1:c.700G>T
|
ENSP00000501242.1:p.Gly234Cys
|
|
ENST00000673991.1:c.1077G>T
|
ENSP00000501033.1:p.Leu359=
|
|
ENST00000226760.5:c.1041G>T
MANE Select
|
ENSP00000226760.1:p.Leu347=
|
|
ENST00000503569.5:c.1041G>T
|
ENSP00000423337.1:p.Leu347=
|
|
ENST00000506362.1:c.674G>T
|
|
|
ENST00000507765.1:n.1226G>T
|
|
|
NM_001145853.1:c.1041G>T
|
NP_001139325.1:p.Leu347=
|
|
NM_006005.3:c.1041G>T
MANE Select
|
NP_005996.2:p.Leu347=
|
|
XM_017008586.1:c.1050G>T
|
XP_016864075.1:p.Leu350=
|
|