ENST00000281928.9:c.5627T>A
MANE Select
|
ENSP00000281928.3:p.Leu1876Gln
|
|
ENST00000548694.2:n.617T>A
|
|
|
ENST00000648379.1:n.3995T>A
|
|
|
ENST00000648737.1:n.5391T>A
|
|
|
ENST00000648825.1:n.3812T>A
|
|
|
ENST00000648916.1:n.3638T>A
|
|
|
ENST00000649607.1:c.3811T>A
|
|
|
ENST00000649775.1:c.2116T>A
|
|
|
ENST00000650226.1:c.5663T>A
|
ENSP00000496981.1:p.Leu1888Gln
|
|
ENST00000281928.7:c.5627T>A
|
ENSP00000281928.3:p.Leu1876Gln
|
|
ENST00000548694.1:n.617T>A
|
|
|
ENST00000552447.1:c.240T>A
|
|
|
NM_015335.4:c.5627T>A
|
NP_056150.1:p.Leu1876Gln
|
|
XM_011538080.1:c.5663T>A
|
XP_011536382.1:p.Leu1888Gln
|
|
XM_011538081.1:c.5660T>A
|
XP_011536383.1:p.Leu1887Gln
|
|
XM_011538082.1:c.5633T>A
|
XP_011536384.1:p.Leu1878Gln
|
|
XM_011538080.2:c.5663T>A
|
XP_011536382.1:p.Leu1888Gln
|
|
XM_011538081.2:c.5660T>A
|
XP_011536383.1:p.Leu1887Gln
|
|
XM_011538082.2:c.5633T>A
|
XP_011536384.1:p.Leu1878Gln
|
|
XM_017019090.1:c.5624T>A
|
XP_016874579.1:p.Leu1875Gln
|
|
NM_015335.5:c.5627T>A
MANE Select
|
NP_056150.1:p.Leu1876Gln
|
|