ENST00000336411.7:c.1473T>G
|
ENSP00000337915.3:p.Leu491=
|
|
ENST00000651162.1:n.815T>G
|
|
|
ENST00000651514.1:c.1380T>G
MANE Select
|
ENSP00000498939.1:p.Leu460=
|
|
ENST00000651783.1:c.921T>G
|
ENSP00000498924.1:p.Leu307=
|
|
ENST00000652018.1:c.1233T>G
|
ENSP00000498733.1:p.Leu411=
|
|
ENST00000336411.6:c.1380T>G
|
ENSP00000337915.2:p.Leu460=
|
|
ENST00000354593.6:c.930T>G
|
ENSP00000346607.2:p.Leu310=
|
|
NM_001202855.2:c.1377T>G
|
NP_001189784.1:p.Leu459=
|
|
NM_017460.5:c.1380T>G
|
NP_059488.2:p.Leu460=
|
|
XM_011515841.1:c.1473T>G
|
XP_011514143.1:p.Leu491=
|
|
XM_011515842.1:c.1470T>G
|
XP_011514144.1:p.Leu490=
|
|
NM_017460.6:c.1380T>G
MANE Select
|
NP_059488.2:p.Leu460=
|
|
NM_001202855.3:c.1377T>G
|
NP_001189784.1:p.Leu459=
|
|