ENST00000636937.2:c.2242T>A
|
ENSP00000516154.1:p.Trp748Arg
|
|
ENST00000268124.11:c.2242T>A
MANE Select
|
ENSP00000268124.5:p.Trp748Arg
|
|
ENST00000530292.3:c.1843T>A
|
ENSP00000432885.2:p.Trp615Arg
|
|
ENST00000635986.2:c.2242T>A
|
ENSP00000490653.2:p.Trp748Arg
|
|
ENST00000636774.1:c.*809T>A
|
ENSP00000489799.1:n.*809T>A
|
|
ENST00000637238.1:c.939T>A
|
ENSP00000490756.1:n.939T>A
|
|
ENST00000637264.1:c.1314T>A
|
|
|
ENST00000666746.1:c.1819T>A
|
|
|
ENST00000670281.1:c.562T>A
|
ENSP00000499709.1:p.Trp188Arg
|
|
ENST00000672071.1:n.2440T>A
|
|
|
ENST00000672923.2:n.2345T>A
|
|
|
ENST00000268124.9:c.2242T>A
|
ENSP00000268124.5:p.Trp748Arg
|
|
ENST00000442287.6:c.2242T>A
|
ENSP00000399851.2:p.Trp748Arg
|
|
ENST00000526314.2:c.539+388T>A
|
|
|
ENST00000526398.1:c.391T>A
|
|
|
ENST00000528881.2:c.11T>A
|
|
|
ENST00000530715.5:c.1T>A
|
ENSP00000431395.1:p.Trp1Arg
|
|
ENST00000532584.5:n.444T>A
|
|
|
ENST00000631044.2:c.*1666T>A
|
ENSP00000486730.1:n.*1666T>A
|
|
NM_001126131.1:c.2242T>A
|
NP_001119603.1:p.Trp748Arg
|
|
NM_002693.2:c.2242T>A
|
NP_002684.1:p.Trp748Arg
|
|
NM_001126131.2:c.2242T>A
|
NP_001119603.1:p.Trp748Arg
|
|
NM_002693.3:c.2242T>A
MANE Select
|
NP_002684.1:p.Trp748Arg
|
|