ENST00000369409.9:c.384G>T
|
ENSP00000358417.5:p.Met128Ile
|
|
ENST00000462324.2:n.467G>T
|
|
|
ENST00000641023.2:c.384G>T
MANE Select
|
ENSP00000493175.1:p.Met128Ile
|
|
ENST00000641074.1:c.384G>T
|
ENSP00000493446.1:p.Met128Ile
|
|
ENST00000641115.1:c.384G>T
|
ENSP00000493264.1:p.Met128Ile
|
|
ENST00000641213.1:c.*37G>T
|
ENSP00000493079.1:n.*37G>T
|
|
ENST00000641247.1:c.*103G>T
|
ENSP00000492955.1:n.*103G>T
|
|
ENST00000641272.1:c.318G>T
|
ENSP00000493432.1:p.Met106Ile
|
|
ENST00000641314.1:n.369G>T
|
|
|
ENST00000641371.1:c.298G>T
|
ENSP00000493305.1:p.Glu100Ter
|
|
ENST00000641375.1:c.*220G>T
|
ENSP00000493089.1:n.*220G>T
|
|
ENST00000641491.1:c.*37G>T
|
ENSP00000493187.1:n.*37G>T
|
|
ENST00000641513.1:c.*128G>T
|
ENSP00000493398.1:n.*128G>T
|
|
ENST00000641570.1:c.*103G>T
|
ENSP00000493213.1:n.*103G>T
|
|
ENST00000641573.1:n.472G>T
|
|
|
ENST00000641587.1:c.*95G>T
|
ENSP00000493453.1:n.*95G>T
|
|
ENST00000641597.1:c.384G>T
|
ENSP00000493382.1:p.Met128Ile
|
|
ENST00000641711.1:n.608G>T
|
|
|
ENST00000641756.1:c.*128G>T
|
ENSP00000493147.1:n.*128G>T
|
|
ENST00000641811.1:c.140G>T
|
|
|
ENST00000641847.1:n.243G>T
|
|
|
ENST00000641891.1:c.*210G>T
|
ENSP00000493288.1:n.*210G>T
|
|
ENST00000641927.1:n.324G>T
|
|
|
ENST00000641947.1:c.384G>T
|
ENSP00000492994.1:p.Met128Ile
|
|
ENST00000642021.1:n.506G>T
|
|
|
ENST00000642041.1:c.*423G>T
|
ENSP00000493415.1:n.*423G>T
|
|
ENST00000369407.3:c.282G>T
|
ENSP00000358415.3:p.Met94Ile
|
|
ENST00000369409.8:c.384G>T
|
ENSP00000358417.4:p.Met128Ile
|
|
ENST00000462324.1:n.652G>T
|
|
|
ENST00000493622.5:n.573G>T
|
|
|
NM_006623.3:c.384G>T
|
NP_006614.2:p.Met128Ile
|
|
XM_011541226.1:c.606G>T
|
XP_011539528.1:p.Met202Ile
|
|
XM_011541227.1:c.528G>T
|
XP_011539529.1:p.Met176Ile
|
|
XM_011541228.1:c.495G>T
|
XP_011539530.1:p.Met165Ile
|
|
XM_011541229.1:c.321G>T
|
XP_011539531.1:p.Met107Ile
|
|
XM_011541230.1:c.99G>T
|
XP_011539532.1:p.Met33Ile
|
|
XM_011541231.1:c.90G>T
|
XP_011539533.1:p.Met30Ile
|
|
XM_011541226.2:c.606G>T
|
XP_011539528.1:p.Met202Ile
|
|
XM_011541227.2:c.528G>T
|
XP_011539529.1:p.Met176Ile
|
|
XM_011541228.2:c.495G>T
|
XP_011539530.1:p.Met165Ile
|
|
XM_011541231.2:c.90G>T
|
XP_011539533.1:p.Met30Ile
|
|
XM_024446338.1:c.495G>T
|
XP_024302106.1:p.Met165Ile
|
|
NM_006623.4:c.384G>T
MANE Select
|
NP_006614.2:p.Met128Ile
|
|