ENST00000333213.11:c.691C>T
MANE Select
|
ENSP00000327487.6:p.Pro231Ser
|
|
ENST00000434205.8:c.388C>T
|
ENSP00000406559.4:p.Pro130Ser
|
|
ENST00000545228.3:c.691C>T
|
ENSP00000438169.3:p.Pro231Ser
|
|
ENST00000579449.2:n.490C>T
|
|
|
ENST00000580013.6:n.894C>T
|
|
|
ENST00000583818.2:c.745C>T
|
ENSP00000461928.2:n.745C>T
|
|
ENST00000679370.1:n.1272C>T
|
|
|
ENST00000679429.1:c.*149C>T
|
ENSP00000505403.1:n.*149C>T
|
|
ENST00000679443.1:n.760C>T
|
|
|
ENST00000679782.1:c.691C>T
|
ENSP00000505995.1:p.Pro231Ser
|
|
ENST00000679919.1:n.760C>T
|
|
|
ENST00000679928.1:c.*302C>T
|
ENSP00000506071.1:n.*302C>T
|
|
ENST00000680528.1:n.716C>T
|
|
|
ENST00000680999.1:c.691C>T
|
ENSP00000504984.1:p.Pro231Ser
|
|
ENST00000681282.1:c.720C>T
|
ENSP00000506339.1:p.Ala240=
|
|
ENST00000333213.10:c.691C>T
|
ENSP00000327487.6:p.Pro231Ser
|
|
ENST00000578415.1:c.651C>T
|
|
|
ENST00000583173.5:c.459-235C>T
|
ENSP00000463619.1:n.459-235C>T
|
|
ENST00000583818.1:c.640C>T
|
ENSP00000461928.1:n.640C>T
|
|
NM_207346.2:c.691C>T
|
NP_997229.2:p.Pro231Ser
|
|
XM_005257229.2:c.691C>T
|
XP_005257286.1:p.Pro231Ser
|
|
XM_006721821.2:c.388C>T
|
XP_006721884.1:p.Pro130Ser
|
|
XM_011524616.1:c.691C>T
|
XP_011522918.1:p.Pro231Ser
|
|
XM_011524617.1:c.691C>T
|
XP_011522919.1:p.Pro231Ser
|
|
XM_011524618.1:c.691C>T
|
XP_011522920.1:p.Pro231Ser
|
|
XR_243646.2:n.721C>T
|
|
|
XM_005257229.4:c.691C>T
|
XP_005257286.1:p.Pro231Ser
|
|
XR_243646.4:n.727C>T
|
|
|
NM_207346.3:c.691C>T
MANE Select
|
NP_997229.2:p.Pro231Ser
|
|