ENST00000700555.2:n.704T>G
|
|
|
ENST00000700557.2:n.293T>G
|
|
|
ENST00000700559.2:c.2168-3534T>G
|
ENSP00000515065.2:n.2168-3534T>G
|
|
ENST00000546498.2:n.888T>G
|
|
|
ENST00000549461.2:n.693T>G
|
|
|
ENST00000700555.1:c.632T>G
|
ENSP00000515062.1:p.Ile211Ser
|
|
ENST00000700556.1:c.672T>G
|
|
|
ENST00000700557.1:c.212T>G
|
ENSP00000515064.1:p.Ile71Ser
|
|
ENST00000700558.1:n.415T>G
|
|
|
ENST00000700559.1:c.1383-3534T>G
|
|
|
ENST00000700560.1:n.1416T>G
|
|
|
ENST00000700561.1:n.1542T>G
|
|
|
ENST00000070846.11:c.2333T>G
|
ENSP00000070846.6:p.Ile778Ser
|
|
ENST00000340811.9:c.2201T>G
MANE Select
|
ENSP00000342800.5:p.Ile734Ser
|
|
ENST00000070846.10:c.2333T>G
|
ENSP00000070846.6:p.Ile778Ser
|
|
ENST00000340811.8:c.2201T>G
|
ENSP00000342800.4:p.Ile734Ser
|
|
ENST00000613243.1:c.2333T>G
|
ENSP00000478295.1:p.Ile778Ser
|
|
NM_001005242.2:c.2201T>G
|
NP_001005242.2:p.Ile734Ser
|
|
NM_004572.3:c.2333T>G , LRG_398t1:c.2333T>G
|
NP_004563.2:p.Ile778Ser
|
|
NM_001005242.3:c.2201T>G
MANE Select
|
NP_001005242.2:p.Ile734Ser
|
|
NM_004572.4:c.2333T>G
|
NP_004563.2:p.Ile778Ser
|
|