ENST00000320694.13:c.703A>T
|
ENSP00000323512.8:p.Ile235Phe
|
|
ENST00000336483.10:c.793A>T
|
ENSP00000338554.5:p.Ile265Phe
|
|
ENST00000517643.2:c.1603A>T
|
ENSP00000513333.1:p.Ile535Phe
|
|
ENST00000517698.6:c.*573A>T
|
ENSP00000430424.1:n.*573A>T
|
|
ENST00000521657.6:c.1603A>T
|
ENSP00000429277.1:p.Ile535Phe
|
|
ENST00000522084.6:c.793A>T
|
ENSP00000429766.2:p.Ile265Phe
|
|
ENST00000697457.1:c.1528A>T
|
ENSP00000513315.1:p.Ile510Phe
|
|
ENST00000697458.1:c.1603A>T
|
ENSP00000513316.1:p.Ile535Phe
|
|
ENST00000697460.1:c.1078A>T
|
ENSP00000513318.1:p.Ile360Phe
|
|
ENST00000697461.1:c.1603A>T
|
ENSP00000513319.1:p.Ile535Phe
|
|
ENST00000697462.1:c.793A>T
|
ENSP00000513320.1:p.Ile265Phe
|
|
ENST00000697463.1:n.1244A>T
|
|
|
ENST00000697464.1:c.*569A>T
|
ENSP00000513322.1:n.*569A>T
|
|
ENST00000697465.1:c.640A>T
|
ENSP00000513323.1:p.Ile214Phe
|
|
ENST00000697466.1:c.610A>T
|
ENSP00000513324.1:p.Ile204Phe
|
|
ENST00000697467.1:c.514A>T
|
ENSP00000513325.1:p.Ile172Phe
|
|
ENST00000697468.1:c.586A>T
|
ENSP00000513326.1:p.Ile196Phe
|
|
ENST00000697469.1:c.295A>T
|
ENSP00000513327.1:p.Ile99Phe
|
|
ENST00000697470.1:c.199A>T
|
ENSP00000513328.1:p.Ile67Phe
|
|
ENST00000697557.1:c.586A>T
|
ENSP00000513335.1:p.Ile196Phe
|
|
ENST00000521381.6:c.1603A>T
MANE Select
|
ENSP00000428056.1:p.Ile535Phe
|
|
ENST00000320694.12:c.703A>T
|
ENSP00000323512.8:p.Ile235Phe
|
|
ENST00000336483.9:c.793A>T
|
ENSP00000338554.5:p.Ile265Phe
|
|
ENST00000517698.5:c.*573A>T
|
ENSP00000430424.1:n.*573A>T
|
|
ENST00000518813.5:n.2146A>T
|
|
|
ENST00000520550.1:n.1002A>T
|
|
|
ENST00000521381.5:c.1603A>T
|
ENSP00000428056.1:p.Ile535Phe
|
|
ENST00000521657.5:c.1603A>T
|
ENSP00000429277.1:p.Ile535Phe
|
|
ENST00000523872.1:c.514A>T
|
ENSP00000430098.1:p.Ile172Phe
|
|
NM_001242466.1:c.514A>T
|
NP_001229395.1:p.Ile172Phe
|
|
NM_181504.3:c.793A>T
|
NP_852556.2:p.Ile265Phe
|
|
NM_181523.2:c.1603A>T
|
NP_852664.1:p.Ile535Phe
|
|
NM_181524.1:c.703A>T
|
NP_852665.1:p.Ile235Phe
|
|
XM_005248542.2:c.1603A>T
|
XP_005248599.1:p.Ile535Phe
|
|
XM_011543493.1:c.1276A>T
|
XP_011541795.1:p.Ile426Phe
|
|
XM_005248542.3:c.1603A>T
|
XP_005248599.1:p.Ile535Phe
|
|
XM_011543493.3:c.1276A>T
|
XP_011541795.1:p.Ile426Phe
|
|
XM_017009585.2:c.1603A>T
|
XP_016865074.1:p.Ile535Phe
|
|
XM_017009586.1:c.1330A>T
|
XP_016865075.1:p.Ile444Phe
|
|
NM_181523.3:c.1603A>T
MANE Select
|
NP_852664.1:p.Ile535Phe
|
|
NM_001242466.2:c.514A>T
|
NP_001229395.1:p.Ile172Phe
|
|
NM_181504.4:c.793A>T
|
NP_852556.2:p.Ile265Phe
|
|
NM_181524.2:c.703A>T
|
NP_852665.1:p.Ile235Phe
|
|