ENST00000405460.9:c.11528T>C
MANE Select
|
ENSP00000384582.2:p.Ile3843Thr
|
|
ENST00000425867.3:c.659T>C
|
ENSP00000392618.3:p.Ile220Thr
|
|
ENST00000639431.1:c.265+78924T>C
|
ENSP00000491057.1:n.265+78924T>C
|
|
ENST00000640374.1:n.4672T>C
|
|
|
ENST00000640464.1:n.1947T>C
|
|
|
ENST00000405460.6:c.11528T>C
|
ENSP00000384582.2:p.Ile3843Thr
|
|
ENST00000509621.1:c.4225T>C
|
|
|
NM_032119.3:c.11528T>C
|
NP_115495.3:p.Ile3843Thr
|
|
NR_003149.1:n.11541T>C
|
|
|
XM_011543675.1:c.11525T>C
|
XP_011541977.1:p.Ile3842Thr
|
|
XM_011543676.1:c.11447T>C
|
XP_011541978.1:p.Ile3816Thr
|
|
XM_011543677.1:c.8831T>C
|
XP_011541979.1:p.Ile2944Thr
|
|
XM_011543678.1:c.11528T>C
|
XP_011541980.1:p.Ile3843Thr
|
|
NM_032119.4:c.11528T>C
MANE Select
|
NP_115495.3:p.Ile3843Thr
|
|
XM_017009963.2:c.11549T>C
|
XP_016865452.1:p.Ile3850Thr
|
|
XM_017009964.2:c.11546T>C
|
XP_016865453.1:p.Ile3849Thr
|
|
XM_017009965.1:c.11546T>C
|
XP_016865454.1:p.Ile3849Thr
|
|
XM_017009966.2:c.11468T>C
|
XP_016865455.1:p.Ile3823Thr
|
|
XM_017009967.1:c.11453T>C
|
XP_016865456.1:p.Ile3818Thr
|
|
XM_017009968.2:c.11549T>C
|
XP_016865457.1:p.Ile3850Thr
|
|
XM_017009969.2:c.11549T>C
|
XP_016865458.1:p.Ile3850Thr
|
|
XM_017009970.2:c.11549T>C
|
XP_016865459.1:p.Ile3850Thr
|
|
XM_017009971.2:c.11549T>C
|
XP_016865460.1:p.Ile3850Thr
|
|
XM_017009972.1:c.4667T>C
|
XP_016865461.1:p.Ile1556Thr
|
|
XM_017009973.1:c.4646T>C
|
XP_016865462.1:p.Ile1549Thr
|
|
NR_003149.2:n.11544T>C
|
|
|