ENST00000249750.9:c.489T>A
MANE Select
|
ENSP00000249750.4:p.Pro163=
|
|
ENST00000249750.8:c.489T>A
|
ENSP00000249750.4:p.Pro163=
|
|
ENST00000347587.7:c.489T>A
|
ENSP00000309623.3:p.Pro163=
|
|
ENST00000430119.6:c.*463T>A
|
ENSP00000416754.2:n.*463T>A
|
|
ENST00000537372.5:c.426T>A
|
ENSP00000438296.1:p.Pro142=
|
|
ENST00000558231.5:c.402T>A
|
ENSP00000453600.1:p.Pro134=
|
|
ENST00000559266.5:n.318+3205T>A
|
|
|
ENST00000559517.5:c.201T>A
|
ENSP00000453408.1:p.Pro67=
|
|
ENST00000561070.5:c.201T>A
|
ENSP00000452850.1:p.Pro67=
|
|
NM_001206897.1:c.426T>A
|
NP_001193826.1:p.Pro142=
|
|
NM_003888.3:c.489T>A
|
NP_003879.2:p.Pro163=
|
|
NM_170696.2:c.489T>A
|
NP_733797.1:p.Pro163=
|
|
NM_170697.2:c.201T>A
|
NP_733798.1:p.Pro67=
|
|
XM_024450095.1:c.489T>A
|
XP_024305863.1:p.Pro163=
|
|
NM_003888.4:c.489T>A
MANE Select
|
NP_003879.2:p.Pro163=
|
|
NM_170696.3:c.489T>A
|
NP_733797.1:p.Pro163=
|
|
NM_170697.3:c.201T>A
|
NP_733798.1:p.Pro67=
|
|
NM_001206897.2:c.426T>A
|
NP_001193826.1:p.Pro142=
|
|