ENST00000336411.7:c.1454T>A
|
ENSP00000337915.3:p.Leu485His
|
|
ENST00000651162.1:n.796T>A
|
|
|
ENST00000651514.1:c.1361T>A
MANE Select
|
ENSP00000498939.1:p.Leu454His
|
|
ENST00000651783.1:c.902T>A
|
ENSP00000498924.1:p.Leu301His
|
|
ENST00000652018.1:c.1214T>A
|
ENSP00000498733.1:p.Leu405His
|
|
ENST00000336411.6:c.1361T>A
|
ENSP00000337915.2:p.Leu454His
|
|
ENST00000354593.6:c.911T>A
|
ENSP00000346607.2:p.Leu304His
|
|
NM_001202855.2:c.1358T>A
|
NP_001189784.1:p.Leu453His
|
|
NM_017460.5:c.1361T>A
|
NP_059488.2:p.Leu454His
|
|
XM_011515841.1:c.1454T>A
|
XP_011514143.1:p.Leu485His
|
|
XM_011515842.1:c.1451T>A
|
XP_011514144.1:p.Leu484His
|
|
NM_017460.6:c.1361T>A
MANE Select
|
NP_059488.2:p.Leu454His
|
|
NM_001202855.3:c.1358T>A
|
NP_001189784.1:p.Leu453His
|
|