|
ENST00000464391.2:n.908G>A
|
|
|
|
ENST00000491889.6:c.*1713G>A
|
ENSP00000419914.1:n.*1713G>A
|
|
|
ENST00000645252.2:n.792G>A
|
|
|
|
ENST00000682749.1:c.1885G>A
|
ENSP00000507306.1:p.Ala629Thr
|
|
|
ENST00000682846.1:c.132-26640G>A
|
ENSP00000507527.1:n.132-26640G>A
|
|
|
ENST00000682864.1:n.849G>A
|
|
|
|
ENST00000381971.8:c.2350G>A
MANE Select
|
ENSP00000371398.3:p.Ala784Thr
|
|
|
ENST00000645252.1:n.792G>A
|
|
|
|
ENST00000324333.14:c.1885G>A
|
ENSP00000325494.10:p.Ala629Thr
|
|
|
ENST00000381971.7:c.2350G>A
|
ENSP00000371398.3:p.Ala784Thr
|
|
|
ENST00000461870.5:n.706G>A
|
|
|
|
ENST00000467497.6:n.890G>A
|
|
|
|
NM_001042413.1:c.2350G>A
|
NP_001035878.1:p.Ala784Thr
|
|
|
NM_152629.3:c.1885G>A
|
NP_689842.3:p.Ala629Thr
|
|
|
XM_005251386.3:c.1885G>A
|
XP_005251443.1:p.Ala629Thr
|
|
|
XM_005251387.3:c.1684G>A
|
XP_005251444.1:p.Ala562Thr
|
|
|
XM_005251388.3:c.1684G>A
|
XP_005251445.1:p.Ala562Thr
|
|
|
XM_011517763.1:c.2350G>A
|
XP_011516065.1:p.Ala784Thr
|
|
|
XM_011517764.1:c.2350G>A
|
XP_011516066.1:p.Ala784Thr
|
|
|
XM_011517765.1:c.2350G>A
|
XP_011516067.1:p.Ala784Thr
|
|
|
XM_011517766.1:c.1885G>A
|
XP_011516068.1:p.Ala629Thr
|
|
|
XM_011517767.1:c.1684G>A
|
XP_011516069.1:p.Ala562Thr
|
|
|
XM_005251386.4:c.1885G>A
|
XP_005251443.1:p.Ala629Thr
|
|
|
XM_005251387.4:c.1684G>A
|
XP_005251444.1:p.Ala562Thr
|
|
|
XM_005251388.4:c.1684G>A
|
XP_005251445.1:p.Ala562Thr
|
|
|
XM_011517763.2:c.2350G>A
|
XP_011516065.1:p.Ala784Thr
|
|
|
XM_011517764.2:c.2350G>A
|
XP_011516066.1:p.Ala784Thr
|
|
|
XM_011517765.2:c.2350G>A
|
XP_011516067.1:p.Ala784Thr
|
|
|
XM_011517766.2:c.1885G>A
|
XP_011516068.1:p.Ala629Thr
|
|
|
XM_011517767.3:c.1684G>A
|
XP_011516069.1:p.Ala562Thr
|
|
|
XM_017014361.1:c.1885G>A
|
XP_016869850.1:p.Ala629Thr
|
|
|
NM_001042413.2:c.2350G>A
MANE Select
|
NP_001035878.1:p.Ala784Thr
|
|
|
NM_152629.4:c.1885G>A
|
NP_689842.3:p.Ala629Thr
|
|
