ENST00000336411.7:c.1469T>C
|
ENSP00000337915.3:p.Val490Ala
|
|
ENST00000651162.1:n.811T>C
|
|
|
ENST00000651514.1:c.1376T>C
MANE Select
|
ENSP00000498939.1:p.Val459Ala
|
|
ENST00000651783.1:c.917T>C
|
ENSP00000498924.1:p.Val306Ala
|
|
ENST00000652018.1:c.1229T>C
|
ENSP00000498733.1:p.Val410Ala
|
|
ENST00000336411.6:c.1376T>C
|
ENSP00000337915.2:p.Val459Ala
|
|
ENST00000354593.6:c.926T>C
|
ENSP00000346607.2:p.Val309Ala
|
|
NM_001202855.2:c.1373T>C
|
NP_001189784.1:p.Val458Ala
|
|
NM_017460.5:c.1376T>C
|
NP_059488.2:p.Val459Ala
|
|
XM_011515841.1:c.1469T>C
|
XP_011514143.1:p.Val490Ala
|
|
XM_011515842.1:c.1466T>C
|
XP_011514144.1:p.Val489Ala
|
|
NM_017460.6:c.1376T>C
MANE Select
|
NP_059488.2:p.Val459Ala
|
|
NM_001202855.3:c.1373T>C
|
NP_001189784.1:p.Val458Ala
|
|