ENST00000269217.11:c.3458A>T
MANE Plus Clinical
|
ENSP00000269217.5:p.Glu1153Val
|
|
ENST00000313654.14:c.8285A>T
MANE Select
|
ENSP00000324532.8:p.Glu2762Val
|
|
ENST00000649721.1:c.4880A>T
|
ENSP00000497885.1:p.Glu1627Val
|
|
ENST00000269217.10:c.3458A>T
|
ENSP00000269217.5:p.Glu1153Val
|
|
ENST00000313654.13:c.8285A>T
|
ENSP00000324532.8:p.Glu2762Val
|
|
ENST00000399516.7:c.8117A>T
|
ENSP00000382432.2:p.Glu2706Val
|
|
ENST00000586751.5:c.3063A>T
|
|
|
ENST00000587184.5:c.3290A>T
|
ENSP00000466557.1:p.Glu1097Val
|
|
ENST00000588770.5:n.2863A>T
|
|
|
NM_000227.4:c.3458A>T
|
NP_000218.3:p.Glu1153Val
|
|
NM_001127717.2:c.8117A>T
|
NP_001121189.2:p.Glu2706Val
|
|
NM_001127718.2:c.3290A>T
|
NP_001121190.2:p.Glu1097Val
|
|
NM_198129.2:c.8285A>T
|
NP_937762.2:p.Glu2762Val
|
|
XM_011525978.1:c.8312A>T
|
XP_011524280.1:p.Glu2771Val
|
|
XM_011525979.1:c.8303A>T
|
XP_011524281.1:p.Glu2768Val
|
|
XM_011525980.1:c.8294A>T
|
XP_011524282.1:p.Glu2765Val
|
|
XM_011525981.1:c.8180A>T
|
XP_011524283.1:p.Glu2727Val
|
|
XM_011525982.1:c.8015A>T
|
XP_011524284.1:p.Glu2672Val
|
|
XM_011525978.2:c.8312A>T
|
XP_011524280.1:p.Glu2771Val
|
|
XM_011525979.2:c.8303A>T
|
XP_011524281.1:p.Glu2768Val
|
|
XM_011525980.2:c.8294A>T
|
XP_011524282.1:p.Glu2765Val
|
|
XM_011525981.2:c.8180A>T
|
XP_011524283.1:p.Glu2727Val
|
|
XM_011525982.2:c.8015A>T
|
XP_011524284.1:p.Glu2672Val
|
|
XM_017025743.1:c.6164A>T
|
XP_016881232.1:p.Glu2055Val
|
|
XM_017025744.1:c.3854A>T
|
XP_016881233.1:p.Glu1285Val
|
|
XR_001753199.1:n.8553A>T
|
|
|
NM_000227.5:c.3458A>T
|
NP_000218.3:p.Glu1153Val
|
|
NM_001127717.3:c.8117A>T
|
NP_001121189.2:p.Glu2706Val
|
|
NM_001127718.3:c.3290A>T
|
NP_001121190.2:p.Glu1097Val
|
|
NM_198129.3:c.8285A>T
|
NP_937762.2:p.Glu2762Val
|
|
NM_000227.6:c.3458A>T
MANE Plus Clinical
|
NP_000218.3:p.Glu1153Val
|
|
NM_001127717.4:c.8117A>T
|
NP_001121189.2:p.Glu2706Val
|
|
NM_001127718.4:c.3290A>T
|
NP_001121190.2:p.Glu1097Val
|
|
NM_198129.4:c.8285A>T
MANE Select
|
NP_937762.2:p.Glu2762Val
|
|