ENST00000700555.2:n.436T>G
|
|
|
ENST00000700559.2:c.1933T>G
|
ENSP00000515065.2:p.Leu645Val
|
|
ENST00000700563.2:c.1933T>G
|
ENSP00000515066.2:p.Leu645Val
|
|
ENST00000546498.2:n.620T>G
|
|
|
ENST00000549461.2:n.472T>G
|
|
|
ENST00000700555.1:c.364T>G
|
ENSP00000515062.1:p.Leu122Val
|
|
ENST00000700556.1:c.404T>G
|
|
|
ENST00000700558.1:n.147T>G
|
|
|
ENST00000700559.1:c.1148T>G
|
|
|
ENST00000700560.1:n.1148T>G
|
|
|
ENST00000700561.1:n.1274T>G
|
|
|
ENST00000700562.1:n.471T>G
|
|
|
ENST00000700563.1:c.1887T>G
|
|
|
ENST00000700564.1:n.1937T>G
|
|
|
ENST00000070846.11:c.2065T>G
|
ENSP00000070846.6:p.Leu689Val
|
|
ENST00000340811.9:c.1933T>G
MANE Select
|
ENSP00000342800.5:p.Leu645Val
|
|
ENST00000070846.10:c.2065T>G
|
ENSP00000070846.6:p.Leu689Val
|
|
ENST00000340811.8:c.1933T>G
|
ENSP00000342800.4:p.Leu645Val
|
|
ENST00000549461.1:n.379T>G
|
|
|
ENST00000552612.5:n.354T>G
|
|
|
ENST00000613243.1:c.2065T>G
|
ENSP00000478295.1:p.Leu689Val
|
|
NM_001005242.2:c.1933T>G
|
NP_001005242.2:p.Leu645Val
|
|
NM_004572.3:c.2065T>G , LRG_398t1:c.2065T>G
|
NP_004563.2:p.Leu689Val
|
|
NM_001005242.3:c.1933T>G
MANE Select
|
NP_001005242.2:p.Leu645Val
|
|
NM_004572.4:c.2065T>G
|
NP_004563.2:p.Leu689Val
|
|