ENST00000405460.9:c.10867G>A
MANE Select
|
ENSP00000384582.2:p.Val3623Ile
|
|
ENST00000639431.1:c.265+69479G>A
|
ENSP00000491057.1:n.265+69479G>A
|
|
ENST00000640374.1:n.4011G>A
|
|
|
ENST00000640464.1:n.1286G>A
|
|
|
ENST00000405460.6:c.10867G>A
|
ENSP00000384582.2:p.Val3623Ile
|
|
ENST00000509621.1:c.3564G>A
|
|
|
NM_032119.3:c.10867G>A
|
NP_115495.3:p.Val3623Ile
|
|
NR_003149.1:n.10880G>A
|
|
|
XM_011543675.1:c.10864G>A
|
XP_011541977.1:p.Val3622Ile
|
|
XM_011543676.1:c.10786G>A
|
XP_011541978.1:p.Val3596Ile
|
|
XM_011543677.1:c.8170G>A
|
XP_011541979.1:p.Val2724Ile
|
|
XM_011543678.1:c.10867G>A
|
XP_011541980.1:p.Val3623Ile
|
|
NM_032119.4:c.10867G>A
MANE Select
|
NP_115495.3:p.Val3623Ile
|
|
XM_017009963.2:c.10888G>A
|
XP_016865452.1:p.Val3630Ile
|
|
XM_017009964.2:c.10885G>A
|
XP_016865453.1:p.Val3629Ile
|
|
XM_017009965.1:c.10885G>A
|
XP_016865454.1:p.Val3629Ile
|
|
XM_017009966.2:c.10807G>A
|
XP_016865455.1:p.Val3603Ile
|
|
XM_017009967.1:c.10792G>A
|
XP_016865456.1:p.Val3598Ile
|
|
XM_017009968.2:c.10888G>A
|
XP_016865457.1:p.Val3630Ile
|
|
XM_017009969.2:c.10888G>A
|
XP_016865458.1:p.Val3630Ile
|
|
XM_017009970.2:c.10888G>A
|
XP_016865459.1:p.Val3630Ile
|
|
XM_017009971.2:c.10888G>A
|
XP_016865460.1:p.Val3630Ile
|
|
XM_017009972.1:c.4006G>A
|
XP_016865461.1:p.Val1336Ile
|
|
XM_017009973.1:c.3985G>A
|
XP_016865462.1:p.Val1329Ile
|
|
NR_003149.2:n.10883G>A
|
|
|