|
ENST00000481058.2:n.195G>T
(ADAM9)
|
|
|
|
ENST00000487273.7:c.45G>T
(ADAM9)
MANE Select
|
ENSP00000419446.2:p.Arg15=
|
|
|
ENST00000676489.1:n.134G>T
(ADAM9)
|
|
|
|
ENST00000676617.1:c.45G>T
(ADAM9)
|
ENSP00000504583.1:p.Arg15=
|
|
|
ENST00000676643.1:c.45G>T
(ADAM9)
|
ENSP00000503079.1:p.Arg15=
|
|
|
ENST00000676669.1:c.45G>T
(ADAM9)
|
ENSP00000503215.1:p.Arg15=
|
|
|
ENST00000676765.1:c.45G>T
(ADAM9)
|
ENSP00000503374.1:p.Arg15=
|
|
|
ENST00000676936.1:c.45G>T
(ADAM9)
|
ENSP00000504471.1:p.Arg15=
|
|
|
ENST00000677004.1:c.45G>T
(ADAM9)
|
ENSP00000503932.1:p.Arg15=
|
|
|
ENST00000677137.1:c.45G>T
(ADAM9)
|
ENSP00000502895.1:p.Arg15=
|
|
|
ENST00000677165.1:c.45G>T
(ADAM9)
|
ENSP00000502865.1:p.Arg15=
|
|
|
ENST00000677359.1:c.45G>T
(ADAM9)
|
ENSP00000504373.1:p.Arg15=
|
|
|
ENST00000677582.1:c.45G>T
(ADAM9)
|
ENSP00000503648.1:p.Arg15=
|
|
|
ENST00000677908.1:c.45G>T
(ADAM9)
|
ENSP00000504640.1:p.Arg15=
|
|
|
ENST00000678253.1:c.45G>T
(ADAM9)
|
ENSP00000503454.1:p.Arg15=
|
|
|
ENST00000678474.1:c.45G>T
(ADAM9)
|
ENSP00000503418.1:p.Arg15=
|
|
|
ENST00000678540.1:c.45G>T
(ADAM9)
|
ENSP00000503206.1:p.Arg15=
|
|
|
ENST00000678730.1:c.45G>T
(ADAM9)
|
ENSP00000503523.1:p.Arg15=
|
|
|
ENST00000679268.1:c.45G>T
(ADAM9)
|
ENSP00000503584.1:p.Arg15=
|
|
|
ENST00000379917.7:c.45G>T
(ADAM9)
|
ENSP00000369249.3:p.Arg15=
|
|
|
ENST00000466936.5:c.45G>T
(ADAM9)
|
ENSP00000420257.1:p.Arg15=
|
|
|
ENST00000468065.5:c.45G>T
(ADAM9)
|
ENSP00000418737.1:p.Arg15=
|
|
|
ENST00000481513.5:c.45G>T
(ADAM9)
|
ENSP00000417066.1:p.Arg15=
|
|
|
ENST00000481873.7:c.45G>T
(ADAM9)
|
ENSP00000418437.3:p.Arg15=
|
|
|
ENST00000487273.6:c.45G>T
(ADAM9)
|
ENSP00000419446.2:p.Arg15=
|
|
|
NM_003816.2:c.45G>T
(ADAM9)
|
NP_003807.1:p.Arg15=
|
|
|
NR_027638.1:n.123G>T
(ADAM9)
|
|
|
|
NR_027639.1:n.123G>T
(ADAM9)
|
|
|
|
NR_027878.1:n.123G>T
(ADAM9)
|
|
|
|
XR_949497.1:n.144G>T
(ADAM9)
|
|
|
|
XM_011544667.2:c.-706C>A
(TM2D2)
|
XP_011542969.1:n.-706C>A
|
|
|
XR_001745616.2:n.342G>T
(ADAM9)
|
|
|
|
XR_001745618.2:n.342G>T
(ADAM9)
|
|
|
|
NM_003816.3:c.45G>T
(ADAM9)
MANE Select
|
NP_003807.1:p.Arg15=
|
|
|
NR_027638.2:n.136G>T
(ADAM9)
|
|
|
|
NR_027639.2:n.136G>T
(ADAM9)
|
|
|
|
NR_027878.2:n.136G>T
(ADAM9)
|
|
|
