ENST00000405460.9:c.10868T>C
MANE Select
|
ENSP00000384582.2:p.Val3623Ala
|
|
ENST00000639431.1:c.265+69480T>C
|
ENSP00000491057.1:n.265+69480T>C
|
|
ENST00000640374.1:n.4012T>C
|
|
|
ENST00000640464.1:n.1287T>C
|
|
|
ENST00000405460.6:c.10868T>C
|
ENSP00000384582.2:p.Val3623Ala
|
|
ENST00000509621.1:c.3565T>C
|
|
|
NM_032119.3:c.10868T>C
|
NP_115495.3:p.Val3623Ala
|
|
NR_003149.1:n.10881T>C
|
|
|
XM_011543675.1:c.10865T>C
|
XP_011541977.1:p.Val3622Ala
|
|
XM_011543676.1:c.10787T>C
|
XP_011541978.1:p.Val3596Ala
|
|
XM_011543677.1:c.8171T>C
|
XP_011541979.1:p.Val2724Ala
|
|
XM_011543678.1:c.10868T>C
|
XP_011541980.1:p.Val3623Ala
|
|
NM_032119.4:c.10868T>C
MANE Select
|
NP_115495.3:p.Val3623Ala
|
|
XM_017009963.2:c.10889T>C
|
XP_016865452.1:p.Val3630Ala
|
|
XM_017009964.2:c.10886T>C
|
XP_016865453.1:p.Val3629Ala
|
|
XM_017009965.1:c.10886T>C
|
XP_016865454.1:p.Val3629Ala
|
|
XM_017009966.2:c.10808T>C
|
XP_016865455.1:p.Val3603Ala
|
|
XM_017009967.1:c.10793T>C
|
XP_016865456.1:p.Val3598Ala
|
|
XM_017009968.2:c.10889T>C
|
XP_016865457.1:p.Val3630Ala
|
|
XM_017009969.2:c.10889T>C
|
XP_016865458.1:p.Val3630Ala
|
|
XM_017009970.2:c.10889T>C
|
XP_016865459.1:p.Val3630Ala
|
|
XM_017009971.2:c.10889T>C
|
XP_016865460.1:p.Val3630Ala
|
|
XM_017009972.1:c.4007T>C
|
XP_016865461.1:p.Val1336Ala
|
|
XM_017009973.1:c.3986T>C
|
XP_016865462.1:p.Val1329Ala
|
|
NR_003149.2:n.10884T>C
|
|
|