ENST00000697149.1:c.1622G>A
|
ENSP00000513138.1:n.1622G>A
|
|
ENST00000697150.1:c.1680G>A
|
ENSP00000513139.1:n.1680G>A
|
|
ENST00000697151.1:c.1613G>A
|
ENSP00000513140.1:n.1613G>A
|
|
ENST00000697164.1:c.1693G>A
|
ENSP00000513153.1:p.Val565Ile
|
|
ENST00000697165.1:c.1480G>A
|
ENSP00000513154.1:p.Val494Ile
|
|
ENST00000347310.10:c.1783G>A
MANE Select
|
ENSP00000321345.5:p.Val595Ile
|
|
ENST00000637002.1:c.1174G>A
|
ENSP00000490340.1:p.Val392Ile
|
|
ENST00000347310.9:c.1783G>A
|
ENSP00000321345.5:p.Val595Ile
|
|
ENST00000395227.2:c.577G>A
|
ENSP00000378652.2:p.Val193Ile
|
|
ENST00000425614.3:c.1018G>A
|
ENSP00000387640.2:p.Val340Ile
|
|
ENST00000473881.2:c.*609G>A
|
ENSP00000486667.1:n.*609G>A
|
|
NM_144701.2:c.1783G>A
|
NP_653302.2:p.Val595Ile
|
|
XM_005270516.2:c.1021G>A
|
XP_005270573.1:p.Val341Ile
|
|
XM_011540789.1:c.1873G>A
|
XP_011539091.1:p.Val625Ile
|
|
XM_011540790.1:c.1783G>A
|
XP_011539092.1:p.Val595Ile
|
|
XM_011540791.1:c.1783G>A
|
XP_011539093.1:p.Val595Ile
|
|
XM_011540790.3:c.1783G>A
|
XP_011539092.1:p.Val595Ile
|
|
XM_011540791.3:c.1783G>A
|
XP_011539093.1:p.Val595Ile
|
|
XR_001736993.1:n.1863G>A
|
|
|
NM_144701.3:c.1783G>A
MANE Select
|
NP_653302.2:p.Val595Ile
|
|