ENST00000697953.1:n.245G>T
|
|
|
ENST00000698016.1:c.216G>T
|
ENSP00000513502.1:p.Leu72=
|
|
ENST00000698021.1:c.20G>T
|
|
|
ENST00000698022.1:c.174G>T
|
ENSP00000513504.1:p.Leu58=
|
|
ENST00000698027.1:c.216G>T
|
ENSP00000513505.1:p.Leu72=
|
|
ENST00000448276.7:c.357G>T
MANE Select
|
ENSP00000392617.2:p.Leu119=
|
|
ENST00000225742.13:c.132G>T
|
ENSP00000225742.9:p.Leu44=
|
|
ENST00000323347.14:c.213G>T
|
ENSP00000318451.10:p.Leu71=
|
|
ENST00000448276.6:c.357G>T
|
ENSP00000392617.2:p.Leu119=
|
|
ENST00000577686.1:n.53-248G>T
|
|
|
ENST00000580054.1:c.141G>T
|
ENSP00000463793.1:p.Leu47=
|
|
ENST00000584400.5:c.217-248G>T
|
ENSP00000464503.1:n.217-248G>T
|
|
ENST00000613943.4:c.246G>T
|
ENSP00000483605.1:p.Leu82=
|
|
NM_001098426.1:c.357G>T
|
NP_001091896.1:p.Leu119=
|
|
XM_005257604.2:c.132G>T
|
XP_005257661.2:p.Leu44=
|
|
NM_001330439.1:c.132G>T
|
NP_001317368.1:p.Leu44=
|
|
NM_001330440.1:c.213G>T
|
NP_001317369.1:p.Leu71=
|
|
NM_001098426.2:c.357G>T
MANE Select
|
NP_001091896.1:p.Leu119=
|
|
NM_001330440.2:c.213G>T
|
NP_001317369.1:p.Leu71=
|
|