ENST00000336411.7:c.798+119G=
|
ENSP00000337915.3:n.798+119G=
|
|
ENST00000651162.1:n.233+119G=
|
|
|
ENST00000651514.1:c.798+119G=
MANE Select
|
ENSP00000498939.1:n.798+119G=
|
|
ENST00000651783.1:c.339+119G=
|
ENSP00000498924.1:n.339+119G=
|
|
ENST00000652018.1:c.651+119G=
|
ENSP00000498733.1:n.651+119G=
|
|
ENST00000336411.6:c.798+119G=
|
ENSP00000337915.2:n.798+119G=
|
|
ENST00000354593.6:c.348+119G=
|
ENSP00000346607.2:n.348+119G=
|
|
NM_001202855.2:c.795+119G=
|
NP_001189784.1:n.795+119G=
|
|
NM_017460.5:c.798+119G=
|
NP_059488.2:n.798+119G=
|
|
XM_011515841.1:c.798+119G=
|
XP_011514143.1:n.798+119G=
|
|
XM_011515842.1:c.795+119G=
|
XP_011514144.1:n.795+119G=
|
|
NM_017460.6:c.798+119G=
MANE Select
|
NP_059488.2:n.798+119G=
|
|
NM_001202855.3:c.795+119G=
|
NP_001189784.1:n.795+119G=
|
|