ENST00000369409.9:c.417G>T
|
ENSP00000358417.5:p.Met139Ile
|
|
ENST00000462324.2:n.500G>T
|
|
|
ENST00000641023.2:c.417G>T
MANE Select
|
ENSP00000493175.1:p.Met139Ile
|
|
ENST00000641074.1:c.417G>T
|
ENSP00000493446.1:p.Met139Ile
|
|
ENST00000641115.1:c.417G>T
|
ENSP00000493264.1:p.Met139Ile
|
|
ENST00000641213.1:c.*70G>T
|
ENSP00000493079.1:n.*70G>T
|
|
ENST00000641247.1:c.*136G>T
|
ENSP00000492955.1:n.*136G>T
|
|
ENST00000641272.1:c.351G>T
|
ENSP00000493432.1:p.Met117Ile
|
|
ENST00000641314.1:n.402G>T
|
|
|
ENST00000641371.1:c.331G>T
|
ENSP00000493305.1:p.Gly111Trp
|
|
ENST00000641375.1:c.*253G>T
|
ENSP00000493089.1:n.*253G>T
|
|
ENST00000641491.1:c.*70G>T
|
ENSP00000493187.1:n.*70G>T
|
|
ENST00000641570.1:c.*136G>T
|
ENSP00000493213.1:n.*136G>T
|
|
ENST00000641573.1:n.505G>T
|
|
|
ENST00000641587.1:c.*128G>T
|
ENSP00000493453.1:n.*128G>T
|
|
ENST00000641597.1:c.417G>T
|
ENSP00000493382.1:p.Met139Ile
|
|
ENST00000641711.1:n.641G>T
|
|
|
ENST00000641756.1:c.*161G>T
|
ENSP00000493147.1:n.*161G>T
|
|
ENST00000641811.1:c.173G>T
|
|
|
ENST00000641847.1:n.276G>T
|
|
|
ENST00000641891.1:c.*243G>T
|
ENSP00000493288.1:n.*243G>T
|
|
ENST00000641927.1:n.357G>T
|
|
|
ENST00000641947.1:c.417G>T
|
ENSP00000492994.1:p.Met139Ile
|
|
ENST00000642021.1:n.539G>T
|
|
|
ENST00000642041.1:c.*456G>T
|
ENSP00000493415.1:n.*456G>T
|
|
ENST00000369407.3:c.315G>T
|
ENSP00000358415.3:p.Met105Ile
|
|
ENST00000369409.8:c.417G>T
|
ENSP00000358417.4:p.Met139Ile
|
|
ENST00000462324.1:n.685G>T
|
|
|
ENST00000493622.5:n.606G>T
|
|
|
NM_006623.3:c.417G>T
|
NP_006614.2:p.Met139Ile
|
|
XM_011541226.1:c.639G>T
|
XP_011539528.1:p.Met213Ile
|
|
XM_011541227.1:c.561G>T
|
XP_011539529.1:p.Met187Ile
|
|
XM_011541228.1:c.528G>T
|
XP_011539530.1:p.Met176Ile
|
|
XM_011541229.1:c.354G>T
|
XP_011539531.1:p.Met118Ile
|
|
XM_011541230.1:c.132G>T
|
XP_011539532.1:p.Met44Ile
|
|
XM_011541231.1:c.123G>T
|
XP_011539533.1:p.Met41Ile
|
|
XM_011541226.2:c.639G>T
|
XP_011539528.1:p.Met213Ile
|
|
XM_011541227.2:c.561G>T
|
XP_011539529.1:p.Met187Ile
|
|
XM_011541228.2:c.528G>T
|
XP_011539530.1:p.Met176Ile
|
|
XM_011541231.2:c.123G>T
|
XP_011539533.1:p.Met41Ile
|
|
XM_024446338.1:c.528G>T
|
XP_024302106.1:p.Met176Ile
|
|
NM_006623.4:c.417G>T
MANE Select
|
NP_006614.2:p.Met139Ile
|
|