ENST00000336411.7:c.1509+249T=
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ENSP00000337915.3:n.1509+249T=
|
|
ENST00000651162.1:n.851+249T=
|
|
|
ENST00000651514.1:c.1416+249T=
MANE Select
|
ENSP00000498939.1:n.1416+249T=
|
|
ENST00000651783.1:c.957+249T=
|
ENSP00000498924.1:n.957+249T=
|
|
ENST00000652018.1:c.1269+249T=
|
ENSP00000498733.1:n.1269+249T=
|
|
ENST00000336411.6:c.1416+249T=
|
ENSP00000337915.2:n.1416+249T=
|
|
ENST00000354593.6:c.966+249T=
|
ENSP00000346607.2:n.966+249T=
|
|
NM_001202855.2:c.1413+249T=
|
NP_001189784.1:n.1413+249T=
|
|
NM_017460.5:c.1416+249T=
|
NP_059488.2:n.1416+249T=
|
|
XM_011515841.1:c.1509+249T=
|
XP_011514143.1:n.1509+249T=
|
|
XM_011515842.1:c.1506+249T=
|
XP_011514144.1:n.1506+249T=
|
|
NM_017460.6:c.1416+249T=
MANE Select
|
NP_059488.2:n.1416+249T=
|
|
NM_001202855.3:c.1413+249T=
|
NP_001189784.1:n.1413+249T=
|
|