ENST00000340611.9:c.2368G>A
MANE Select
|
ENSP00000339637.4:p.Glu790Lys
|
|
ENST00000340611.8:c.2368G>A
|
ENSP00000339637.4:p.Glu790Lys
|
|
ENST00000467558.5:n.4154G>A
|
|
|
ENST00000469750.5:n.4940G>A
|
|
|
ENST00000493232.5:n.5074G>A
|
|
|
NM_152743.3:c.2368G>A
|
NP_689956.2:p.Glu790Lys
|
|
XM_005249643.3:c.2548G>A
|
XP_005249700.1:p.Glu850Lys
|
|
XM_011515177.1:c.2632G>A
|
XP_011513479.1:p.Glu878Lys
|
|
XM_011515178.1:c.2632G>A
|
XP_011513480.1:p.Glu878Lys
|
|
XM_011515179.1:c.2629G>A
|
XP_011513481.1:p.Glu877Lys
|
|
XM_011515180.1:c.2602G>A
|
XP_011513482.1:p.Glu868Lys
|
|
XM_011515181.1:c.2452G>A
|
XP_011513483.1:p.Glu818Lys
|
|
XM_011515182.1:c.2632G>A
|
XP_011513484.1:p.Glu878Lys
|
|
XM_011515183.1:c.2107G>A
|
XP_011513485.1:p.Glu703Lys
|
|
XM_011515184.1:c.2107G>A
|
XP_011513486.1:p.Glu703Lys
|
|
XM_011515185.1:c.2368G>A
|
XP_011513487.1:p.Glu790Lys
|
|
XM_011515187.1:c.1204G>A
|
XP_011513489.1:p.Glu402Lys
|
|
NM_001350626.1:c.2548G>A
|
NP_001337555.1:p.Glu850Lys
|
|
NM_001350627.1:c.1843G>A
|
NP_001337556.1:p.Glu615Lys
|
|
NR_146879.1:n.2785G>A
|
|
|
XM_011515177.2:c.2632G>A
|
XP_011513479.1:p.Glu878Lys
|
|
XM_011515179.2:c.2629G>A
|
XP_011513481.1:p.Glu877Lys
|
|
XM_011515181.2:c.2452G>A
|
XP_011513483.1:p.Glu818Lys
|
|
XM_011515182.2:c.2632G>A
|
XP_011513484.1:p.Glu878Lys
|
|
XM_011515184.3:c.2107G>A
|
XP_011513486.1:p.Glu703Lys
|
|
XM_011515186.2:c.*515G>A
|
XP_011513488.1:n.*515G>A
|
|
XM_017011833.1:c.2545G>A
|
XP_016867322.1:p.Glu849Lys
|
|
XM_017011834.1:c.2365G>A
|
XP_016867323.1:p.Glu789Lys
|
|
XM_017011836.2:c.*515G>A
|
XP_016867325.1:n.*515G>A
|
|
XM_024446682.1:c.1204G>A
|
XP_024302450.1:p.Glu402Lys
|
|
NM_152743.4:c.2368G>A
MANE Select
|
NP_689956.2:p.Glu790Lys
|
|
NM_001350626.2:c.2548G>A
|
NP_001337555.1:p.Glu850Lys
|
|
NM_001350627.2:c.1843G>A
|
NP_001337556.1:p.Glu615Lys
|
|
NR_146879.2:n.2551G>A
|
|
|