ENST00000636937.2:c.3300G>T
|
ENSP00000516154.1:p.Val1100=
|
|
ENST00000268124.11:c.3300G>T
MANE Select
|
ENSP00000268124.5:p.Val1100=
|
|
ENST00000530292.3:c.2901G>T
|
ENSP00000432885.2:p.Val967=
|
|
ENST00000635986.2:c.*370G>T
|
ENSP00000490653.2:n.*370G>T
|
|
ENST00000636774.1:c.*1867G>T
|
ENSP00000489799.1:n.*1867G>T
|
|
ENST00000637238.1:c.2109G>T
|
ENSP00000490756.1:n.2109G>T
|
|
ENST00000637264.1:c.2372G>T
|
|
|
ENST00000666746.1:c.2877G>T
|
|
|
ENST00000672071.1:n.3498G>T
|
|
|
ENST00000672695.1:n.477G>T
|
|
|
ENST00000672923.2:n.3300G>T
|
|
|
ENST00000268124.9:c.3300G>T
|
ENSP00000268124.5:p.Val1100=
|
|
ENST00000442287.6:c.3300G>T
|
ENSP00000399851.2:p.Val1100=
|
|
ENST00000530292.2:c.384G>T
|
ENSP00000432885.1:p.Val128=
|
|
ENST00000631044.2:c.*2724G>T
|
ENSP00000486730.1:n.*2724G>T
|
|
NM_001126131.1:c.3300G>T
|
NP_001119603.1:p.Val1100=
|
|
NM_002693.2:c.3300G>T
|
NP_002684.1:p.Val1100=
|
|
NM_001126131.2:c.3300G>T
|
NP_001119603.1:p.Val1100=
|
|
NM_002693.3:c.3300G>T
MANE Select
|
NP_002684.1:p.Val1100=
|
|