ENST00000700555.2:n.703A>T
|
|
|
ENST00000700557.2:n.292A>T
|
|
|
ENST00000700559.2:c.2168-3535A>T
|
ENSP00000515065.2:n.2168-3535A>T
|
|
ENST00000546498.2:n.887A>T
|
|
|
ENST00000549461.2:n.692A>T
|
|
|
ENST00000700555.1:c.631A>T
|
ENSP00000515062.1:p.Ile211Phe
|
|
ENST00000700556.1:c.671A>T
|
|
|
ENST00000700557.1:c.211A>T
|
ENSP00000515064.1:p.Ile71Phe
|
|
ENST00000700558.1:n.414A>T
|
|
|
ENST00000700559.1:c.1383-3535A>T
|
|
|
ENST00000700560.1:n.1415A>T
|
|
|
ENST00000700561.1:n.1541A>T
|
|
|
ENST00000070846.11:c.2332A>T
|
ENSP00000070846.6:p.Ile778Phe
|
|
ENST00000340811.9:c.2200A>T
MANE Select
|
ENSP00000342800.5:p.Ile734Phe
|
|
ENST00000070846.10:c.2332A>T
|
ENSP00000070846.6:p.Ile778Phe
|
|
ENST00000340811.8:c.2200A>T
|
ENSP00000342800.4:p.Ile734Phe
|
|
ENST00000613243.1:c.2332A>T
|
ENSP00000478295.1:p.Ile778Phe
|
|
NM_001005242.2:c.2200A>T
|
NP_001005242.2:p.Ile734Phe
|
|
NM_004572.3:c.2332A>T , LRG_398t1:c.2332A>T
|
NP_004563.2:p.Ile778Phe
|
|
NM_001005242.3:c.2200A>T
MANE Select
|
NP_001005242.2:p.Ile734Phe
|
|
NM_004572.4:c.2332A>T
|
NP_004563.2:p.Ile778Phe
|
|