ENST00000700555.2:n.655C>G
|
|
|
ENST00000700557.2:n.244C>G
|
|
|
ENST00000700559.2:c.2152C>G
|
ENSP00000515065.2:p.Leu718Val
|
|
ENST00000546498.2:n.839C>G
|
|
|
ENST00000549461.2:n.659+32C>G
|
|
|
ENST00000700555.1:c.583C>G
|
ENSP00000515062.1:p.Leu195Val
|
|
ENST00000700556.1:c.623C>G
|
|
|
ENST00000700557.1:c.163C>G
|
ENSP00000515064.1:p.Leu55Val
|
|
ENST00000700558.1:n.366C>G
|
|
|
ENST00000700559.1:c.1367C>G
|
|
|
ENST00000700560.1:n.1367C>G
|
|
|
ENST00000700561.1:n.1493C>G
|
|
|
ENST00000070846.11:c.2284C>G
|
ENSP00000070846.6:p.Leu762Val
|
|
ENST00000340811.9:c.2152C>G
MANE Select
|
ENSP00000342800.5:p.Leu718Val
|
|
ENST00000070846.10:c.2284C>G
|
ENSP00000070846.6:p.Leu762Val
|
|
ENST00000340811.8:c.2152C>G
|
ENSP00000342800.4:p.Leu718Val
|
|
ENST00000613243.1:c.2284C>G
|
ENSP00000478295.1:p.Leu762Val
|
|
NM_001005242.2:c.2152C>G
|
NP_001005242.2:p.Leu718Val
|
|
NM_004572.3:c.2284C>G , LRG_398t1:c.2284C>G
|
NP_004563.2:p.Leu762Val
|
|
NM_001005242.3:c.2152C>G
MANE Select
|
NP_001005242.2:p.Leu718Val
|
|
NM_004572.4:c.2284C>G
|
NP_004563.2:p.Leu762Val
|
|