|
NM_005120.3:c.4159A>G
MANE Select
|
NP_005111.2:p.Ile1387Val
|
|
ENST00000374080.8:c.4159A>G
MANE Select
|
ENSP00000363193.3:p.Ile1387Val
|
|
NM_005120.2:c.4159A>G
|
NP_005111.2:p.Ile1387Val
|
|
ENST00000333646.10:c.3700A>G
|
ENSP00000333125.7:p.Ile1234Val
|
|
ENST00000333646.11:c.4039A>G
|
ENSP00000333125.8:p.Ile1347Val
|
|
ENST00000374080.7:c.4159A>G
|
ENSP00000363193.3:p.Ile1387Val
|
|
ENST00000374102.5:c.4159A>G
|
ENSP00000363215.1:p.Ile1387Val
|
|
ENST00000374102.6:c.4159A>G
|
ENSP00000363215.2:p.Ile1387Val
|
|
ENST00000685182.1:n.792A>G
|
|
|
ENST00000685655.1:c.112A>G
|
ENSP00000509298.1:p.Ile38Val
|
|
ENST00000686169.1:n.536A>G
|
|
|
ENST00000686548.1:c.*4055A>G
|
ENSP00000509582.1:n.*4055A>G
|
|
ENST00000687161.1:n.874A>G
|
|
|
ENST00000687382.1:c.4159A>G
|
ENSP00000510724.1:p.Ile1387Val
|
|
ENST00000687701.1:n.788A>G
|
|
|
ENST00000688079.1:n.2154A>G
|
|
|
ENST00000688663.1:c.*1080A>G
|
ENSP00000509348.1:n.*1080A>G
|
|
ENST00000688881.1:n.813A>G
|
|
|
ENST00000688993.1:n.360A>G
|
|
|
ENST00000689768.1:n.2769A>G
|
|
|
ENST00000690145.1:c.4159A>G
|
ENSP00000508818.1:p.Ile1387Val
|
|
ENST00000690242.1:c.4159A>G
|
ENSP00000510090.1:p.Ile1387Val
|
|
ENST00000690250.1:n.1828A>G
|
|
|
ENST00000690690.1:c.612A>G
|
|
|
ENST00000690828.1:n.4415A>G
|
|
|
ENST00000691113.1:c.2638A>G
|
ENSP00000509755.1:n.2638A>G
|
|
ENST00000691426.1:n.3288A>G
|
|
|
ENST00000691468.1:c.4108A>G
|
ENSP00000509011.1:p.Ile1370Val
|
|
ENST00000691909.1:n.879A>G
|
|
|
ENST00000692304.1:c.4159A>G
|
ENSP00000508427.1:p.Ile1387Val
|
|
ENST00000692893.1:n.1468A>G
|
|
|
ENST00000692964.1:n.823A>G
|
|
|
ENST00000693050.1:n.666A>G
|
|
|
ENST00000693324.1:c.4123A>G
|
ENSP00000508643.1:p.Ile1375Val
|
|
ENST00000693391.1:c.2104A>G
|
ENSP00000509563.1:p.Ile702Val
|
|
XM_005262317.1:c.4159A>G
|
XP_005262374.1:p.Ile1387Val
|
|
XM_005262319.1:c.4159A>G
|
XP_005262376.1:p.Ile1387Val
|