ENST00000405460.9:c.9419T>C
MANE Select
|
ENSP00000384582.2:p.Ile3140Thr
|
|
ENST00000639431.1:c.265+40492T>C
|
ENSP00000491057.1:n.265+40492T>C
|
|
ENST00000639473.1:n.4878T>C
|
|
|
ENST00000640012.1:c.3226T>C
|
|
|
ENST00000640374.1:n.2563T>C
|
|
|
ENST00000640779.1:c.4148T>C
|
|
|
ENST00000405460.6:c.9419T>C
|
ENSP00000384582.2:p.Ile3140Thr
|
|
ENST00000509621.1:c.2116T>C
|
|
|
NM_032119.3:c.9419T>C
|
NP_115495.3:p.Ile3140Thr
|
|
NR_003149.1:n.9432T>C
|
|
|
XM_011543675.1:c.9416T>C
|
XP_011541977.1:p.Ile3139Thr
|
|
XM_011543676.1:c.9338T>C
|
XP_011541978.1:p.Ile3113Thr
|
|
XM_011543677.1:c.6722T>C
|
XP_011541979.1:p.Ile2241Thr
|
|
XM_011543678.1:c.9419T>C
|
XP_011541980.1:p.Ile3140Thr
|
|
XM_011543679.1:c.9419T>C
|
XP_011541981.1:p.Ile3140Thr
|
|
XR_948560.1:n.272-892A>G
|
|
|
NM_032119.4:c.9419T>C
MANE Select
|
NP_115495.3:p.Ile3140Thr
|
|
XM_017009963.2:c.9440T>C
|
XP_016865452.1:p.Ile3147Thr
|
|
XM_017009964.2:c.9437T>C
|
XP_016865453.1:p.Ile3146Thr
|
|
XM_017009965.1:c.9437T>C
|
XP_016865454.1:p.Ile3146Thr
|
|
XM_017009966.2:c.9359T>C
|
XP_016865455.1:p.Ile3120Thr
|
|
XM_017009967.1:c.9344T>C
|
XP_016865456.1:p.Ile3115Thr
|
|
XM_017009968.2:c.9440T>C
|
XP_016865457.1:p.Ile3147Thr
|
|
XM_017009969.2:c.9440T>C
|
XP_016865458.1:p.Ile3147Thr
|
|
XM_017009970.2:c.9440T>C
|
XP_016865459.1:p.Ile3147Thr
|
|
XM_017009971.2:c.9440T>C
|
XP_016865460.1:p.Ile3147Thr
|
|
XM_017009972.1:c.2558T>C
|
XP_016865461.1:p.Ile853Thr
|
|
XM_017009973.1:c.2537T>C
|
XP_016865462.1:p.Ile846Thr
|
|
XM_017009974.2:c.9440T>C
|
XP_016865463.1:p.Ile3147Thr
|
|
XR_001742802.1:n.2523-892A>G
|
|
|
NR_003149.2:n.9435T>C
|
|
|