ENST00000700555.2:n.841G>A
|
|
|
ENST00000700557.2:n.430G>A
|
|
|
ENST00000700559.2:c.2168-3397G>A
|
ENSP00000515065.2:n.2168-3397G>A
|
|
ENST00000546498.2:n.1025G>A
|
|
|
ENST00000549461.2:n.830G>A
|
|
|
ENST00000700555.1:c.769G>A
|
ENSP00000515062.1:p.Ala257Thr
|
|
ENST00000700556.1:c.809G>A
|
|
|
ENST00000700557.1:c.349G>A
|
ENSP00000515064.1:p.Ala117Thr
|
|
ENST00000700558.1:n.552G>A
|
|
|
ENST00000700559.1:c.1383-3397G>A
|
|
|
ENST00000700560.1:n.1553G>A
|
|
|
ENST00000700561.1:n.1679G>A
|
|
|
ENST00000070846.11:c.2470G>A
|
ENSP00000070846.6:p.Ala824Thr
|
|
ENST00000340811.9:c.2338G>A
MANE Select
|
ENSP00000342800.5:p.Ala780Thr
|
|
ENST00000070846.10:c.2470G>A
|
ENSP00000070846.6:p.Ala824Thr
|
|
ENST00000340811.8:c.2338G>A
|
ENSP00000342800.4:p.Ala780Thr
|
|
ENST00000613243.1:c.2468G>A
|
ENSP00000478295.1:p.Gly823Asp
|
|
NM_001005242.2:c.2338G>A
|
NP_001005242.2:p.Ala780Thr
|
|
NM_004572.3:c.2470G>A , LRG_398t1:c.2470G>A
|
NP_004563.2:p.Ala824Thr
|
|
NM_001005242.3:c.2338G>A
MANE Select
|
NP_001005242.2:p.Ala780Thr
|
|
NM_004572.4:c.2470G>A
|
NP_004563.2:p.Ala824Thr
|
|